Infobox Disease Name Dilatedcardiomyopathy DiseasesDB 3066 ICD10 ICD10 I 42 0 i 30 ICD9 ICD9 425.4 ICDO ... 80 eMedicine2 ped 2502 MeshID D002311 Dilatedcardiomyopathy or DCM is a condition in which the heart ... information center view0 ref Dilatedcardiomyopathy is the most common form of non Ischemia ... ref About one in three cases of congestive heart failure CHF is due to dilatedcardiomyopathy. ref name Harrisons Dilatedcardiomyopathy also occurs in children. Causes Although in many cases no cause etiology is apparent, dilatedcardiomyopathy is probably the result of damage to the myocardium produced ... TA, Liu P, Sole MJ title Viral infection and the pathogenesis of dilatedcardiomyopathy journal ... are also suggested as a cause for dilatedcardiomyopathy. ref cite journal author San Mart n MA, Garc a A, Rodr guez FJ, Terol I title Dilatedcardiomyopathy and autoimmunity an overview of current ... mrevista cardio.pubmed full?inctrl 05ZI0113&vol 55&num 5&pag 514 ref Dilatedcardiomyopathy can ... medical chronic uncontrolled tachycardia . Many cases of dilatedcardiomyopathy are described ... extrasystole can develop dilatedcardiomyopathy. In these cases, if the extrasystole are reduced or removed ... ref Dilatedcardiomyopathy also occurs more frequently in pregnancy than in the normal population. It occurs .... ref cite journal author Ross J title Dilatedcardiomyopathy concepts derived from gene deficient ... lead to a broken heart the genetics of dilatedcardiomyopathy journal Am J Hum Genet. volume 69 issue ... relatives of patients with dilatedcardiomyopathy have preclinical, asymptomatic heart muscle changes ... Echocardiographic evaluation in asymptomatic relatives of patients with dilatedcardiomyopathy reveals ... MC title Black white differences in idiopathic dilatedcardiomyopathy the Washington DC dilatedCardiomyopathy ... DMD Xp21.2 Associated symptoms For many affected individuals, dilatedcardiomyopathy is a condition ... to cardiomyopathies of non ischemic origin, such as idiopathic dilatedcardiomyopathy or chronic ... more details
isbn 9781849963046 pages 158 ref The most common form of cardiomyopathy is dilatedcardiomyopathy ..., alcoholism has been identified as a cause for some forms of dilatedcardiomyopathy. To make a diagnosis of an intrinsic cardiomyopathy, significant coronary artery disease should be ruled out amongst other things . The term intrinsic cardiomyopathy does not describe the specific etiology of weakened ... of cardiomyopathy you have. Dilatedcardiomyopathy If you re diagnosed with dilatedcardiomyopathy .... Another option for some people with dilatedcardiomyopathy is a special pacemaker that coordinates ...Infobox disease Name Cardiomyopathy Image Idiopathic cardiomyopathy, gross pathology 20G0018 lores.jpg Caption Opened left ventricle of heart shows a thickened, dilated left ventricle with subendocardial ... ICD9 ICD9 425.4 ICDO OMIM MedlinePlus 001105 eMedicineSubj eMedicineTopic MeshID D009202 Cardiomyopathy ... i.e., the actual heart muscle for any reason. People with cardiomyopathy are often at risk of arrhythmia ... 0 07 139140 1 ref Cardiomyopathy can often go undetected, making it especially dangerous to carriers ... cardiomyopathy could apply to almost any disease affecting the heart, in practice it is usually ... 841 Full text ref An extrinsic cardiomyopathy is a cardiomyopathy where the primary pathology is outside ... of a cardiomyopathy is ischemia . The World Health Organization calls these specific cardiomyopathies ref name ref2 An intrinsic cardiomyopathy is defined as weakness in the muscle of the heart that is not due ... cardiomyopathy HCM or HOCM Arrhythmogenic right ventricular cardiomyopathy ARVC Isolated ventricular non compaction Mitochondrial myopathy Mixed Dilatedcardiomyopathy DCM Restrictive cardiomyopathy RCM Acquired Takotsubo cardiomyopathy Loeffler endocarditis Secondary extrinsic cardiomyopathies ... cardiomyopathy hyperthyroidism acromegaly Toxicity chemotherapy Alcoholic cardiomyopathy Neuromuscular muscular dystrophy Nutritional disease s Obesity associated cardiomyopathy ref Improvement ... more details
Infobox disease Name Restrictive cardiomyopathy a.k.a Obliterative cardiomyopathy Image Cardiac amyloidosis very high mag.jpg Caption Micrograph of cardiac amyloidosis , a cause of restrictive cardiomyopathy . Congo red stain . DiseasesDB 11390 ICD10 ICD10 I 42 5 i 30 ICD9 ICD9 425.4 ICDO OMIM MedlinePlus 000189 eMedicineSubj med eMedicineTopic 291 MeshID D002313 Restrictive cardiomyopathy RCM a.k.a Obliterative cardiomyopathy, once known as constrictive cardiomyopathy ref name Hancock cite journal last Hancock first EW title Differential diagnosis of restrictive cardiomyopathy and constrictive pericarditis journal Heart British Cardiac Society date 2001 Sep volume 86 issue 3 pages 343 9 pmid 11514495 url http heart.bmj.com.beckerproxy.wustl.edu content 86 3 343.extract accessdate 15 October 2011 pmc 1729880 ref is a form of cardiomyopathy in which the walls are rigid, ref DorlandsDict two 000017373 restrictive cardiomyopathy ref and the heart is restricted from stretching and filling with blood properly. It is the least common of Goodwin s three original subtypes of cardiomyopathy, which includes hypertrophic cardiomyopathy hypertrophic and dilatedcardiomyopathydilated as well as restrictive ... enter the heart is backed up in the circulatory system. In time, restrictive cardiomyopathy patients ... ref Treatment Therapy for restrictive cardiomyopathy is limited. ref name urlRestrictive CardiomyopathyCardiomyopathy Merck Manual Home Health Handbook cite web url http www.merckmanuals.com home heart and blood vessel disorders cardiomyopathy restrictive cardiomyopathy.html title Restrictive CardiomyopathyCardiomyopathy Merck Manual Home Health Handbook work accessdate 2009 01 04 ref Diuretics ... diastolic function in selected individuals. Heart failure resulting from restrictive cardiomyopathy ... links http www.merckmanuals.com home heart and blood vessel disorders cardiomyopathy overview of cardiomyopathy.html Overview at Merck Manual Circulatory system pathology Category Cardiomyopathy med stub ... more details
Refimprove date May 2011 Infobox musical artist See Wikipedia WikiProject Musicians name Dilated Peoples image Dilated Peoples mika.jpg caption Hamburg Germany 11.Sept.2001 image size background group ... members notable instruments Dilated Peoples is an United States American hip hop group from Los Angeles ... www.allbusiness.com retail trade miscellaneous retail retail stores not 4618780 1.html Dilated Peoples ... copies in the United States. ref http www.billboard.com news dilated peoples back again with new album 1001881107.story news dilated peoples back again with new album 1001881107 Dilated Peoples Back ... Singles & Albums The fourth album, 20 20 Dilated Peoples album 20 20 , was released in 2006 the debut ... . 20 20 Dilated Peoples album 20 20 was the group s farewell album on Capitol Records , ending ..., who originated in Anaheim, California Anaheim . Collaborations Dilated Peoples are affiliated with fellow ... one appearance on each Dilated Peoples album Ear Drums Pop Remix on The Platform Defari Interlude on Expansion Team Closed Session on Neighborhood Watch and Olde English on 20 20 . Dilated Peoples also made multiple appearances on Defari s album Odds & Evens . Another Dilated associate is their long ... , four songs on Neighborhood Watch , and two songs on 20 20 . Dilated Peoples was featured on a song ... Radio, Evidence discussed the status of Dilated Peoples and their relationship as a group. He also ... artist dilated peoples chart history 360595 ref ref http www.allmusic.com artist dilated peoples p393048 charts awards ref ref http acharts.us performer dilated peoples ref style width ... align center 91 align center 2006 20 20 Dilated Peoples album 20 20 small Released February 21, 2006 ... artist id p393048 label Dilated Peoples http www.dilatedpeoples.com Dilated Peoples Homepage http ... http www.cream.cz ?rozhovor evidence dilated peoples reunion 2010&preview 1 Evidence Interview Reunion of Dilated Peoples? 2010 http www.bouriblog.com bouriblog BouriBlog Evidence Interview http www.bouriblog.com ... more details
A dilated pore also known as a Dilated pore of Winer is a cutaneous condition characterized by a solitary, prominent, Blackhead open comedo on the face or upper trunk of an elderly individual. ref name Andrews cite book author James, William D. Berger, Timothy G. et al. title Andrews Diseases of the Skin Clinical Dermatology publisher Saunders Elsevier location year 2006 pages isbn 0 7216 2921 0 oclc doi accessdate ref rp 675 See also Trichodiscoma List of cutaneous conditions References reflist Epidermal growth stub Tumors of skin appendages Category Epidermal nevi, neoplasms, cysts ... more details
Infobox Disease Name Alcoholic cardiomyopathy Image Caption DiseasesDB ICD10 ICD10 I 42 6 i 30 ICD9 ICD9 425.5 ICDO OMIM MedlinePlus 000174 eMedicineSubj med eMedicineTopic 286 MeshID D002310 Alcoholic cardiomyopathy is a disease in which the chronic long term abuse of alcohol leads to heart failure . ref name pmid12006456 cite journal author Piano MR title Alcoholic cardiomyopathy incidence, clinical characteristics, and pathophysiology journal Chest volume 121 issue 5 pages 1638 50 year 2002 month May pmid 12006456 doi 10.1378 chest.121.5.1638 url http www.chestjournal.org cgi pmidlookup?view long&pmid 12006456 ref Alcoholic cardiomyopathy is a type of dilatedcardiomyopathy . Due to the direct toxic effects of alcohol on heart muscle, the heart is unable to pump blood efficiently, leading to heart failure. It can affect other parts of the body if the heart failure is severe. It is most common in males between the ages of 35 50. Symptoms Symptoms presented by the occurrence of alcoholic cardiomyopathy are the result of the heart failing and usually occur after the disease has progressed to an advanced stage. Therefore the symptoms have a lot in common with other forms of cardiomyopathy . These symptoms can include http www.drugs.com enc alcoholic cardiomyopathy.html Ankle, feet, and leg swelling Overall swelling Loss of appetite Shortness of breath, especially with activity Breathing difficulty while lying down Fatigue, weakness, faintness Decreased alertness or concentration Cough containing mucus, or pink, frothy material Decreased urine output oliguria Need to urinate at night ... of alcohol abuse can confirm the diagnosis. Treatment Treatment for alcoholic cardiomyopathy ... which are commonly used with other forms of cardiomyopathy to reduce the strain on the heart .... Treatment will possibly prevent the heart from further deterioration, and the cardiomyopathy is largely ... Alcohealth Category Cardiomyopathy es Cardiomiopat a alcoh lica it Miocardiopatia alcolica ru ... more details
unreferenced date October 2010 Amyloid cardiomyopathy is heart muscle damage caused by amyloidosis . e.g. familial amyloid cardiomyopathy FAC or TTR amyloid cardiomyopathy ATTR CM med stub circulatory stub Category Cardiomyopathy ... more details
al title Mutations in Cypher ZASP in patients with dilatedcardiomyopathy and left ventricular ... several echocardiograms to confirm. The most common misdiagnoses were dilatedcardiomyopathy ... 2 Cases dilated phase hypertensive cardiomyopathy 1 Case restrictive cardiomyopathy 1 Case The high number of misdiagnoses can be attributed to non compaction cardiomyopathy being first reported ...Infobox Disease Name Noncompaction cardiomyopathy Image Caption DiseasesDB ICD10 ICD9 ICDO OMIM 601493 MedlinePlus eMedicineSubj eMedicineTopic MeshID Non compaction cardiomyopathy NCC , also called spongiform cardiomyopathy , is a rare Congenital disorder congenital cardiomyopathy that affects both ... form of cardiomyopathy journal Circulation volume 108 issue 21 pages 2672 8 year 2003 month November ... first5 Candace. title Non compacted Cardiomyopathy Clinical Echocardiographic Study journal Cardiovasc ... cardiomyopathy results when there is failure of this process of compaction. Because the consequence .... History Non compaction cardiomyopathy was first identified as an isolated condition in 1984 ... of cardiomyopathy cardiomyopathies considers noncompaction cardiomyopathy a genetic cardiomyopathy ... Due to its recent establishment as a diagnosis, and it being unclassified as a cardiomyopathy according ... from advanced heart failure. A similar situation occurred with Hypertrophic cardiomyopathy which ... at different age stages. However it is universally understood that non compaction cardiomyopathy ... url ref Symptoms Subjects symptoms from non compaction cardiomyopathy range widely. It is possible ... Candace. title Non compacted Cardiomyopathy Clinical Echocardiographic Study journal Cardiovasc ... index.php?id 274 title LV Non compaction author The Cardiomyopathy Association date 2007 07 23 format ... capacity and exercise intolerance Two conditions though that are more prevalent in noncompaction cardiomyopathy ... Myotubular cardiomyopathy Barth syndrome Misdiagnosis In a study 2006 Citation needed date June 2008 ... more details
Infobox disease Name Peripartum cardiomyopathy Image Caption DiseasesDB 29243 ICD10 ICD10 O 90 3 o 85 ICD9 ICD9 674.5 ICDO OMIM MedlinePlus eMedicineSubj med eMedicineTopic 292 MeshID Peripartum cardiomyopathy PPCM is a form of dilatedcardiomyopathy that is defined as deterioration in cardiac function ... forms of dilatedcardiomyopathy, PPCM involves systolic dysfunction of the heart with a decrease ... S, et al. title Peripartum cardiomyopathy National Heart, Lung, and Blood Institute and Office of Rare ... Pregnancy associated cardiomyopathy clinical characteristics and a comparison between early and late ... 2050 ref ref name SliwaFett cite journal author Sliwa K, Fett J, Elkayam U title Peripartum cardiomyopathy ... cardiomyopathy journal Crit. Care Med. volume 33 issue 10 Suppl pages S340 6 year 2005 month ... 10.1007 s11936 004 0005 8 author Phillips SD, Warnes CA title Peripartum Cardiomyopathy Current Therapeutic ... cardiomyopathy journal Clin Rev Allergy Immunol volume 23 issue 3 pages 301 24 year 2002 month ... failure. ref name Fett2008 cite journal author Fett JD title Understanding peripartum cardiomyopathy ... RD, Ansari AA, Sundstrom JB, Murphy JG title Unrecognized peripartum cardiomyopathy in Haitian ... failure due to unrecognized peripartum cardiomyopathy journal Crit. Care Med. volume 33 issue ... of postpartum cardiomyopathy initially misdiagnosed for pulmonary embolism journal Can J Anaesth volume ... diagnosis of heart failure in peripartum cardiomyopathy journal Critical Pathways in Cardiology ... NN, et al. title Heart transplantation for peripartum cardiomyopathy a report of three cases and a literature ... in peripartum cardiomyopathy with contemporary treatments journal Am. Heart J. volume 152 issue ... in peripartum cardiomyopathy journal Am. Heart J. volume 140 issue 5 pages 785 91 year 2000 month ... cardiomyopathy Impact of beta blockade Abstract 2500 journal Circulation year 2007 volume 116 issue ... reserve in patients with peripartum cardiomyopathy and recovered left ventricular function ... more details
Infobox disease Name Hypertrophic cardiomyopathy Image Caption DiseasesDB 6373 ICD10 ICD10 I 42 1 i 30 ... 290 eMedicine mult eMedicine2 ped 1102 eMedicine2 radio 129 MeshID D002312 Hypertrophic cardiomyopathy ... content full 93 5 841 ref ref name Maron 2002 cite journal author Maron BJ title Hypertrophic cardiomyopathy ... author Sherrid MV, Chaudhry FA, Swistel DG title Obstructive hypertrophic cardiomyopathy echocardiography ... MA, et al. title Hypertrophic cardiomyopathy. The importance of the site and the extent of hypertrophy ... WG title Hypertrophic cardiomyopathy. Clinical spectrum and treatment journal Circulation journal Circulation ... of Cardiology clinical expert consensus document on hypertrophic cardiomyopathy. A report of the American ... 94 4 850 ref The occurrence of hypertrophic cardiomyopathy is a significant cause of sudden unexpected ... to have a more severe form of hypertrophic cardiomyopathy HCM is frequently asymptomatic until .... ref name slate A cardiomyopathy is a primary disease that affects the muscle of the heart. With hypertrophic cardiomyopathy HCM , the sarcomeres contractile elements in the heart replicate ... with development of familial hypertrophic cardiomyopathy. Signs and symptoms The clinical course ... cardiomyopathy by decreasing ventricular volume and increasing outflow resistance. Risk ... with hypertrophic cardiomyopathy journal British Heart Journal Br Heart J volume 72 issue 6 Suppl ... OMIM2 612124 Hypertrophic cardiomyopathy is inherited as an autosomal dominant trait and is attributed ... cardiomyopathy journal Int J Cardiol volume 96 issue 2 pages 157 63 year 2004 month Aug ... in hypertrophic cardiomyopathy and sudden cardiac death journal Lancet volume 342 issue 8879 pages ... . Dynamic outflow obstruction Listen filename Hypertrophic Cardiomyopathy Echocardiogram Sam.ogg ... motion of the mitral valve in hypertrophic cardiomyopathy based on echocardiographic observations ... outflow tract velocity in obstructive hypertrophic cardiomyopathy journal J Am Coll Cardiol. volume ... more details
Boxer cardiomyopathy also known as Boxer arrhythmogenic right ventricular cardiomyopathy is a disease of the myocardium primarily affecting Boxer dogs . It is characterized by the development of ventricular tachyarrhythmias, resulting in Syncope medicine syncope and sudden cardiac death . Myocardial ... C, Fox PR, Meurs KM, et al. Arrhythmogenic right ventricular cardiomyopathy causing sudden cardiac ... Boxer cardiomyopathy shares striking similarities to a human myocardial disease called arrhythmogenic right ventricular cardiomyopathy ARVC . ref name Basso On histopathology, the disease is characterized ... with fatty or fibro fatty tissue. ref name update Meurs KM. Boxer dog cardiomyopathy An update. Vet ... Boxer cardiomyopathy is a genetic disease inherited in an autosomal dominant pattern. ref name familial ... has announced that they have identified one genetic anomaly associated with Boxer cardiomyopathy ref Meurs et al. Abstract Boxer Cardiomyopathy Journal Veterinary Internal Medicine 2009 23 687 688 ref ... debate over the discovery. Clinical presentation Boxer cardiomyopathy is an adult onset ... name update Sudden cardiac death All dogs with Boxer cardiomyopathy are at risk of sudden cardiac .... ref name kittleson Kittleson MD, Kienle RD. Arrhythmogenic Right Ventricular Cardiomyopathy. In Small ... test for Boxer cardiomyopathy is now commercially available. ref Anon. Genetic Mutation Testing Service for Boxer Dog s Arrhythmogenic Right Ventricular Cardiomyopathy Veterinary Cardiac Genetics ... Current treatment options for Boxer cardiomyopathy are largely restricted to the use of oral anti ... 4A 49I 57I. ref The ideal therapy for Boxer cardiomyopathy would be implantation of an implantable cardioverter ... Defibrillator in a Boxer to Control Clinical Signs of Arrhythmogenic Right Ventricular Cardiomyopathy ... cardiomyopathy. ref name nelson References See Wikipedia Footnotes on how to create references using ... DEFAULTSORT Boxer Cardiomyopathy Category Dog diseases ... more details
Infobox disease Name Takotsubo cardiomyopathy Image TakoTsubo scheme.png Caption Schematic representation of takotsubo cardiomyopathy A compared to the situation in a normal person B . DiseasesDB 33976 ... cardiomyopathy. Image Takotsubo ultrasound.gif thumb A Echocardiograph showing dilatation ... ST segment ST and T wave changes from a patient with confirmed takotsubo cardiomyopathy. Takotsubo cardiomyopathy , also known as transient apical ballooning syndrome , ref name pmid18599137 Cite ... article S0167 5273 2808 2900574 3 abstract ref apical ballooning cardiomyopathy , ref name pmid18678857 ... ballooning cardiomyopathy associated with duloxetine journal Ann. Intern. Med. volume 149 issue 3 pages 218 9 year 2008 month August pmid 18678857 doi url ref stress induced cardiomyopathy , Gebrochenes Herz Syndrom , and simply stress cardiomyopathy , is a type of non Ischemia ischaemic cardiomyopathy ... In 1 Of 10 Patients Bot generated title ref Stress cardiomyopathy is a well recognized cause of acute ... journal title Stress Cardiomyopathy journal Annual Review of Medicine author Akashi YJ, Nef HM, Mollmann ... The typical presentation of someone with takotsubo cardiomyopathy is a sudden onset of congestive ... last Gianni first M title Apical ballooning syndrome or takotsubo cardiomyopathy a systematic review ... of individuals with takotsubo cardiomyopathy typically includes a coronary angiogram , which ... improves within 2 months. Takotsubo cardiomyopathy is more commonly seen in post menopausal women .... ref name Azzarelli 2006 Etiology The etiology of takotsubo cardiomyopathy is not fully understood ... that this anatomical variant is not common enough to explain takotsubo cardiomyopathy. ref Cite journal last Inoue first M title Differentiation between patients with takotsubo cardiomyopathy and those ..., S, Gori, M, Sutherland, GG title Tako Tsubo cardiomyopathy new insights into the possible underlying ... patients develop takotsubo cardiomyopathy after an emotional stress, while others have a preceding clinical ... more details
Synthesis date March 2011 Diabetic cardiomyopathy is a disorder of the myocardium heart muscle in people with diabetes mellitus diabetes . It can lead to inability of the heart to circulate blood through the body effectively, a state known as heart failure , with accumulation of fluid in the lung s pulmonary ... from coronary artery disease , and diabetic cardiomyopathy is only said to exist if there is no coronary ... Avogaro A, Vigili de Kreutzenberg S, Negut C, Tiengo A, Scognamiglio R title Diabetic cardiomyopathy ... ref when the hypertrophy and fibrosis become very pronounced. Pathophysiology Diabetic cardiomyopathy ... Fonarow GC, Srikanthan P title Diabetic cardiomyopathy journal Endocrinol. Metab. Clin. North Am. volume ... journal author Severson DL title Diabetic cardiomyopathy recent evidence from mouse models of type ... between myocardial perfusion and dysfunction in diabetic cardiomyopathy a study of quantitative contrast ... Rubler S, Dlugash J, Yuceoglu YZ, Kumral T, Branwood AW, Grishman A title New type of cardiomyopathy ... A critical role for PPARalpha mediated lipotoxicity in the pathogenesis of diabetic cardiomyopathy ..., metabolic remodeling precedes the cardiomyopathy ref cite journal author Buchanan J, Mazumder PK ... animal models with metabolic modulators at an early age, prior to any sign of cardiomyopathy, improvements ... physiology in diabetic cardiomyopathy journal Endocrinol. Metab. Clin. North Am. volume 35 issue ... Ca 2 transport in streptozotocin induced diabetic cardiomyopathy in rats journal Am. J. Physiol. volume ... Ca 2 signaling contributes to cardiomyopathy in Type 1 diabetic rats journal Am. J. Physiol. Heart ... J, Schuster I, et al. title Mechanisms of chem Ca 2 i transient decrease in cardiomyopathy of db db ... cardiomyopathy. Treatment centers around intense glycemic control through diet, oral hypoglycemics ... between increased glycemia and risk of developing diabetic cardiomyopathy, therefore, keeping glucose ... Cardiomyopathy Category Cardiomyopathy Category Diabetes ... more details
Dilated fundus examination DFE is a diagnosis Diagnostic procedure diagnostic procedure that employs the use of mydriasis Mydriatics mydriatic eye drop s such as tropicamide to pupillary response dilate or enlarge the pupil in order to obtain a better view of the fundus eye fundus of the human eye eye . ref http www.aarphealthcare.com prodsvcs eye AARP Exam info.aspx Exam Information Bot generated title ref Once the pupil is dilated, examiners often use specialized equipment such as an ophthalmoscope or fundus camera to view the inner surfaces of the eye. DFE has been found to be a more effective method for evaluation of internal ocular health than non dilated examination. ref cite journal last1 Parisi first1 ML last2 Scheiman first2 M last3 Coulter first3 RS title Comparison of the effectiveness of a nondilated versus dilated fundus examination in the pediatric population journal Journal of the American Optometric Association volume 67 issue 5 pages 266 72 year 1996 pmid 8888844 ref It is frequently performed by ophthalmologist s and optometrist s as part of an eye examination . gallery Image Same eye.jpg An eye prior to dilation Image Result of Dilated fundus examination.JPG Pupil of the same eye in its dilated state gallery References Reflist Category Eye procedures treatment stub Eye procedures bg fr Fond d il ... more details
20 20 Dilated Peoples Album Category 2006 albums Category Dilated Peoples albums Category Capitol ... 20 20 album fr 20 20 album des Dilated Peoples it 20 20 Dilated Peoples ... more details
Infobox disease ICD10 ICD10 I 42 9 i 30 Tachycardia induced cardiomyopathy , also known as chronotropic cardiomyopathy and tachycardiomyopathy , is a weakening of the myocardium the muscle of the heart that is due to prolonged periods of a tachycardia fast heart rate . The rate and duration of the elevation in heart rate necessary to cause a cardiomyopathy is unclear and is likely dependent on a number of unknown factors. Treatment The primary treatment for a tachycardia induced cardiomyopathy is correct the underlying tachycardia. Supportive agents such as beta blocker s and ACE inhibitor s Angiotensin II receptor antagonist angiotensin receptor blockers are of benefit to try to prevent remodeling of the left ventricle . If the tachycardia can be abolished, the heart muscle can recover after some time. ref cite journal author Calo L, Sciarra L, Scioli R, Lamberti F, Loricchio ML, Pandozi C, Santini M. title Recovery of cardiac function after ablation of atrial tachycardia arising from the tricuspid annulus. journal Ital Heart J. year 2005 volume 6 issue 8 pages 652 7 pmid 16161499 ref Not only is there a need to control the tachycardia that is responsible for causing tachycardia induced cardiomyopathy, but also treating underlying conditions that cause tachycardia. For instance, treatment of hyperthyroidism can also lead to reversal of tachycardia induced cardiomyopathy. See also Cardiomyopathy Congestive heart failure References reflist Category Cardiomyopathy disease stub ... more details
orphan date March 2009 main Hypertrophic cardiomyopathy Hypertrophic cardiomyopathy , or HCM, is the leading cause of sudden cardiac death SCD in young athletes. HCM is frequently asymptomatic until SCD, and thus its prevention requires screening. Screening by medical history and physical exam are ineffective, indicating heart abnormalities in only 3 of patients who subsequently suffered SCD. However, HCM can be detected with 80 accuracy by echocardiogram s, which may be combined with pre screening by electrocardiogram s ECGs . Routine cardiac screening of athletes has been implemented in Italy since the 1970s, and has resulted in an 89 drop in cases of SCD among screened athletes. In the United States, the American Heart Association has consistently opposed such routine screening. See Harv Sanghavi 2009 for a popular summary of literature and discussion. Description HCM is a genetic disorder that causes the muscle of the heart the myocardium to thicken or muscle hypertrophy hypertrophy without any apparent reason. When the heart thickens and becomes enlarged, particularly at the septum and left ventricle , it can cause dangerous Cardiac arrythmia arrhythmias abnormal heart rhythms . The thickening of the heart makes it harder for blood to leave, forcing the heart to work more vigorously to pump blood. HCM occurs in up to two per 1000 people in the general population, being a primary ... cardiomyopathy , the condition is seen in people of all ages. Studies have shown that HCM ... in a less dilated left ventricle. This in turn leads to a smaller volume of blood leaving the heart ... filename Hypertrophic Cardiomyopathy Echocardiogram Sam.ogg title Example of Echocardiogram description ... 8. Maron BJ Mar 2002 . Hypertrophic cardiomyopathy a systematic review . JAMA 287 10 1308 20. br 9. Maron BJ. Hypertrophic cardiomyopathy. Practical steps for preventing sudden death. Physician Sportsmed ..., 276. 3. 199 204. br 12. Maron, B.J., Thompson, P.D. 2002 . Hypertrophic Cardiomyopathy. Physician ... more details
multiple issues cleanup December 2011 copy edit December 2011 wikify December 2011 Familial amyloid cardiomyopathy FAC or Transthyretin TTR Amyloid Cardiomyopathy or TTR amyloid cardiomyopathy ATTR CM results from the aggregation of mutant and or wild type transthyretin protein. ref Jacobson, D. R., Pastore, R. D., Yaghoubian, R., Kane, I., Gallo, G., Buck, F. S. & Buxbaum, J. N. 1997 . Variant sequence transthyretin isoleucine 122 in late onset cardiac amyloidosis in black Americans. The New England journal of medicine 336, 466 73. ref Both mutant and wild type transthyretin comprise the aggregates because the TTR blood protein is a tetramer composed of mutant and wild type TTR subunits in heterozygotes. The TTR tetramer has to dissociate in a rate limiting step before the monomer can misfold and become aggregation competent. ref Colon, W. & Kelly, J. W. 1992 . Partial denaturation of transthyretin is sufficient for amyloid fibril formation in vitro. Biochemistry 31, 8654 60. ref Senile systemic amyloidosis, ref Westermark, P., Sletten, K., Johansson, B. & Cornwell, G. G., 3rd. 1990 ... Academy of Sciences of the United States of America 87, 2843 5. ref a highly related cardiomyopathy ... progressing to restrictive cardiomyopathy and heart failure. Several mutations in TTR are primarily ... or with heart blocks. ref Falk, R. H. & Elkayam, U. 2010 . Cardiomyopathy the importance of recognizing ... cardiomyopathy is a combined liver and heart transplan, although treatments aimed at symptom relief ..., that progresses to a cardiomyopathy. ref Coelho, T. 1996 . Familial amyloid polyneuropathy new developments ...., Backman, C., Karp, K. & Suhr, O. B. 2002 . Progression of cardiomyopathy after liver transplantation ... of Familial Amyloid Cardiomyopathy, although this has not been demonstrated by a placebo ... or vyndaqel cardiomyopathy clinical trial has begun http www.clinicaltrials.gov . References reflist ... citations. Amyloidosis Category Cardiomyopathy ... more details
Infobox disease Name Striate palmoplantar keratoderma with woolly hair and cardiomyopathy Image Caption DiseasesDB ICD10 ICD9 ICDO OMIM 605676 MedlinePlus eMedicineSubj eMedicineTopic MeshID Carvajal syndrome also known as Striate palmoplantar keratoderma with woolly hair and cardiomyopathy ref name Bolognia and Striate palmoplantar keratoderma with woolly hair and left ventricular dilatedcardiomyopathy, ref name Fitz2 is a cutaneous condition inherited in an autosomal recessive fashion, and due to a defect in desmoplakin . ref name Bolognia cite book author Rapini, Ronald P. Bolognia, Jean L. Jorizzo, Joseph L. title Dermatology 2 Volume Set publisher Mosby location St. Louis year 2007 pages 811 isbn 1 4160 2999 0 oclc doi accessdate ref Striate palmoplantar keratoderma, woolly hair, and left ventricular dilatedcardiomyopathy has been described in both autosomal dominant and autosomal recessive forms, but only the recessive forms have a clear association with dilatedcardiomyopathy. ref name Fitz2 Freedberg, et al. 2003 . Fitzpatrick s Dermatology in General Medicine . 6th ed. . McGraw Hill. ISBN 0071380760. ref rp 513 The skin disease presents as a striate palmoplantar keratoderma with some nonvolar involvement, particularly at sites of pressure or abrasion. ref name Fitz2 rp 513 See also List of cutaneous conditions References reflist Category Palmoplantar keratodermas Category Genodermatoses Genodermatoses stub Cytoskeletal defects pl Zesp Carvajala ... more details
1G is the first generation wireless telephone technology. 1G or 1 G may also refer to Metallothionein 1G 1g Racing , manufacturer of the Rossion Q1 sports car Astra 1G , a satellite operated by SES S.A. SES SSH 1G WA or Washington State Route 538 Galileo International s IATA code 1G, a model of Toyota G engine See also G force Gram Cardiomyopathy, dilated 1G autosomal dominant G1 disambiguation Letter NumberCombDisambig de 1G ... more details
artery disease CAD and 100 patients with non ischemic cardiomyopathy, mostly idiopathic dilatedcardiomyopathy... ...expanding on patient selection, when the Batista operation was applied without ... more details
merge from Wooly hair date December 2011 Infobox Disease Name PAGENAME Image Caption DiseasesDB ICD10 Q82.5 ILDS Q82.550 ICD9 ICDO OMIM MedlinePlus eMedicineSubj eMedicineTopic MeshID Woolly hair nevus alternatively spelled Wooly hair nevus is a congenital condition in which hair in a circumscribed area of the scalp is kinky or wool woolly . ref name Bolognia cite book author Rapini, Ronald P. Bolognia, Jean L. Jorizzo, Joseph L. title Dermatology 2 Volume Set publisher Mosby location St. Louis year 2007 pages 851 isbn 1 4160 2999 0 oclc doi accessdate ref See also Woolly hair Naxos syndrome Striate palmoplantar keratoderma, woolly hair, and left ventricular dilated cardiomyopathy List of cutaneous conditions References reflist Epidermal growth stub Category Epidermal nevi, neoplasms, cysts Category Conditions of the skin appendages ... more details
?&format F&next images ejour cardio1 cardio1 v18 n3 a4.pdf issn ref and dilatedcardiomyopathy ... death . ref name pmid17612745 Advancement to dilatedcardiomyopathy may be more rapid in patients ... Cardiac troponin T Arg92Trp mutation and progression from hypertrophic to dilatedcardiomyopathy ... T gene shows high degree of penetrance and transition from hypertrophic to dilatedcardiomyopathy journal ... for cardiac troponin T gene mutation detection in familial hypertrophic cardiomyopathy journal Hum. Mutat ... have been associated with familial hypertrophic cardiomyopathy as well as with restrictive cardiomyopathy restrictive ref name pmid17612745 cite journal author Revera M, Van der Merwe L, Heradien ... Mutations in the genes for cardiac troponin T and alpha tropomyosin in hypertrophic cardiomyopathy ... for familial hypertrophic cardiomyopathy maps to chromosome 1q3 journal Nat. Genet. volume 3 issue ... Alpha tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy a disease ... JB, Bachinski LL, Bieling LC, et al. title Localization of a gene responsible for familial dilatedcardiomyopathy to chromosome 1q32 journal Circulation volume 92 issue 12 pages 3387 9 year 1996 pmid ... in familial hypertrophic cardiomyopathy journal Circulation volume 94 issue 12 pages 3069 73 year 1997 ... cardiomyopathy journal J. Mol. Cell. Cardiol. volume 29 issue 2 pages 839 43 year 1997 ... Hypertrophic Cardiomyopathy Overview The PBB Controls template provides controls for Protein Box Bot ... more details
DCM may refer to Technology Data Center http java apps.org content show.php DatacenterManager?content 144298 Manager Deep chlorophyll maximum , subsurface maximum in the concentration of chlorophyll Dichloromethane , a common solvent in organic chemistry Digital Clock Manager , programmed clock signal transformation used in FPGA Digital Imaging and Communications in Medicine filename extension .dcm Direction cosine matrix, see Rotation matrix Discontinuous conduction mode in power electronics see buck converter Dynamic causal modelling , method for the interpretation of functional neuroimaging data Docking Cargo Module , planned Russian module of the International Space Station Drive Configuration Matrix, Western Digital hard drives Other IATA airport code for Castres Mazamet Airport Debt Capital Markets Del Close Marathon Demand chain management Delhi Cloth Mills Denton Corker Marshall , an Australian architecture firm Deputy Chief of Mission Dilated cardiomyopathy Distinguished Conduct Medal , British and Commonwealth medal for extreme bravery NTT DoCoMo s stock symbol on the New York Stock Exchange Doll Capital Management, a Venture Capital firm in Menlo Park, CA, which funded SandForce and others Dunbee Combex Marx Ltd, a former British toy manufacturer which purchased Lines Bros and Schuco Modell disambiguation de DCM fr DCM it DCM ja DCM pl DCM zh DCM ... more details
merge to Woolly hair nevus date December 2011 Wooly hair alternatively spelled Woolly hair is the presence of hair typical of those of sub Saharan ancestry on people from other ethnic backgrounds, hair which, under the microscope, appears tightly coiled, and presents at birth or infancy usually as a solitary inherited trait in an autosomal dominant fashion. ref name Fitz2 Freedberg, et al. 2003 . Fitzpatrick s Dermatology in General Medicine . 6th ed. . McGraw Hill. ISBN 0071380760. ref rp 639 ref name Andrews James, William Berger, Timothy Elston, Dirk 2005 . Andrews Diseases of the Skin Clinical Dermatology . 10th ed. . Saunders. ISBN 0721629210. ref rp 767 8 ref name Bolognia cite book author Rapini, Ronald P. Bolognia, Jean L. Jorizzo, Joseph L. title Dermatology 2 Volume Set publisher Mosby location St. Louis year 2007 pages isbn 1 4160 2999 0 oclc doi accessdate ref See also Wooly hair nevus Naxos syndrome Striate palmoplantar keratoderma, woolly hair, and left ventricular dilated cardiomyopathy List of cutaneous conditions References reflist Category Conditions of the skin appendages skin appendage stub ... more details
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