- Pseudopseudohypoparathyroidism
Infobox disease Name Pseudopseudohypoparathyroidism Image Caption DiseasesDB 29783 ICD10 ICD9 ICD9 275.49 ICDO OMIM 612463 MedlinePlus eMedicineSubj eMedicineTopic MeshID D011556 Pseudopseudohypoparathyroidism pseudoPHP is an inherited disorder, named for its similarity to pseudohypoparathyroidism in presentation. The term pseudopseudohypoparathyroidism is used to describe a condition where the individual has the phenotypic appearance of pseudohypoparathyroidism type 1a, but is biochemically normal. It is sometimes considered a variant of Albright hereditary osteodystrophy . ref name pmid1119829 cite journal author Solomon SS, Kerlan RM, King LE, Jones GM, Hashimoto K title Pseudopseudohypoparathyroidism with fibrous dysplasia journal Arch Dermatol volume 111 issue 1 pages 90 3 year 1975 month January pmid 1119829 doi 10.1001 archderm.111.1.90 url ref It was characterized in 1952 by Fuller ... ref Presentation Pseudopseudohypoparathyroidism can be best understood by comparing it to other conditions ... Skeletal defects normal low gene defect from mother Pseudopseudohypoparathyroidism Skeletal defects ... pages 262 ref gene defect from father Hormone resistance is not present in pseudopseudohypoparathyroidism ... Cognitive impairment is prevalent in pseudohypoparathyroidism type Ia, but not in pseudopseudohypoparathyroidism ... title Military service and pseudopseudohypoparathyroidism recognizing red flags for rare medical conditions ... Obesity is less common in pseudopseudohypoparathyroidism than in pseudohypoparathyroidism. ref name ... Body mass index differences in pseudohypoparathyroidism type 1a versus pseudopseudohypoparathyroidism ... as the presenting feature of albright hereditary osteodystrophy associated with pseudopseudohypoparathyroidism ... 02&page 154 ref Inheritance A mother who has inherited pseudopseudohypoparathyroidism from her father ... s ovum during meiosis. Pseudopseudohypoparathyroidism and pseudohypoparathyroidism both involve ... pmidlookup?view long&pmid 20427508 ref but pseudopseudohypoparathyroidism has normal calcium homeostasis ... more details
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- Progressive osseous heteroplasia
Infobox Disease Name PAGENAME Image Caption DiseasesDB 34694 ICD10 ICD9 ICDO OMIM 166350 MedlinePlus eMedicineSubj eMedicineTopic MeshID Progressive osseous heteroplasia is a cutaneous condition characterized by cutaneous or subcutaneous ossification. 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 It is associated with GNAS . ref name pmid18553568 cite journal author Adegbite NS, Xu M, Kaplan FS, Shore EM, Pignolo RJ title Diagnostic and mutational spectrum of progressive osseous heteroplasia POH and other forms of GNAS based heterotopic ossification journal Am. J. Med. Genet. A volume 146A issue 14 pages 1788 96 year 2008 month July pmid 18553568 pmc 2564798 doi 10.1002 ajmg.a.32346 ref See also Punctate porokeratosis List of cutaneous conditions Pseudopseudohypoparathyroidism References reflist External links Before adding to this list, refer to WP EL and make sure the link complies. Otherwise, it will be deleted. Official websites Please do not add blogs or commercial sites, even if run by CPP. See WP EL. http www.pohdisease.org Progressive Osseous Heteroplasia Association Dermatology stub Deficiencies of intracellular signaling peptides and proteins Category Genodermatoses ... more details
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- Pseudohypoparathyroidism
Suppl 2 pages 635 40 year 2006 month May pmid 16789628 ref Related conditions The term pseudopseudohypoparathyroidism ... hyperphosphatemia elevated parathyroid hormone hyperparathyroidism See also Hypoparathyroidism Pseudopseudohypoparathyroidism ... more details
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- Albright's hereditary osteodystrophy
103580 , whereas paternal inheritance of loss of function mutation results in pseudopseudohypoparathyroidism ... la Suisse romande volume 60 pages 1166 77 year 1940 location Lausanne ref See also Pseudopseudohypoparathyroidism ... more details
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- GNAS complex locus
type Ia pseudopseudohypoparathyroidism McCune Albright syndrome Interactions GNAS complex locus ... more details
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- Parathyroid disease
Pseudohypoparathyroidism Pseudopseudohypoparathyroidism Disorders of the parathyroid hormone receptor ... more details
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- Hypoparathyroidism
, associated with mental retardation and skeleton skeletal deformities and pseudopseudohypoparathyroidism ... hepatitis, and Addison s disease . References references See also Hyperparathyroidism Pseudopseudohypoparathyroidism ... more details
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- Metacarpus
, in pseudohypoparathyroidism and pseudopseudohypoparathyroidism . A blunted fourth metacarpal, with normal ... more details
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- List of MeSH codes (C18)
pseudohypoparathyroidism MeshNumber C18.452.174.766.815 Pseudopseudohypoparathyroidism pseudopseudohypoparathyroidism ... MeshNumber C18.452.648.618.815.815 Pseudopseudohypoparathyroidism pseudopseudohypoparathyroidism ... more details
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- Longest word in English
for the Mary Poppins Mary Poppins film film and Mary Poppins musical musical Coined tt Pseudopseudohypoparathyroidism ... . ref The Oxford English Dictionary contains pseudopseudohypoparathyroidism ... more details
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- List of MeSH codes (C05)
Pseudopseudohypoparathyroidism pseudopseudohypoparathyroidism MeshNumber C05.116.198.762 Renal ... more details
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- List of MeSH codes (C16)
For other categories, see List of MeSH codes . The following is a list of the C codes for MeSH . It is a product of the United States National Library of Medicine . Source for content is http www.nlm.nih.gov mesh filelist.html here . File 2006 MeSH Trees . MeshNumber C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities congenital, hereditary, and neonatal diseases and abnormalities MeshNumber C16.131 Abnormalities abnormalities MeshNumber C16.131.042 Abnormalities, Drug Induced abnormalities, drug induced MeshNumber C16.131.077 Abnormalities, Multiple abnormalities, multiple MeshNumber C16.131.077.065 Alagille Syndrome alagille syndrome MeshNumber C16.131.077.095 Angelman Syndrome angelman syndrome MeshNumber C16.131.077.112 Bardet Biedl Syndrome bardet biedl syndrome MeshNumber C16.131.077.130 Basal Cell Nevus Syndrome basal cell nevus syndrome MeshNumber C16.131.077.133 Beckwith Wiedemann Syndrome beckwith wiedemann syndrome MeshNumber C16.131.077.137 Bloom Syndrome bloom syndrome MeshNumber C16.131.077.208 Branchio Oto Renal Syndrome Branchio Oto Renal Syndrome branchio oto renal syndrome MeshNumber C16.131.077.250 Cockayne Syndrome cockayne syndrome MeshNumber C16.131.077.262 Cri du Chat Syndrome cri du chat syndrome MeshNumber C16.131.077.272 De Lange Syndrome de lange syndrome MeshNumber C16.131.077.327 Down Syndrome down syndrome MeshNumber C16.131.077.350 Ectodermal Dysplasia ectodermal dysplasia MeshNumber C16.131.077.350.398 Ellis Van Creveld Syndrome ellis van creveld syndrome MeshNumber C16.131.077.350.424 Focal Dermal Hypoplasia focal dermal hypoplasia MeshNumber C16.131.077.350.712 Neurocutaneous Syndromes neurocutaneous syndromes MeshNumber C16.131.077.393 Gardner Syndrome gardner syndrome MeshNumber C16.131.077.410 Holoprosencephaly holoprosencephaly MeshNumber C16.131.077.445 Incontinentia Pigmenti incontinentia pigmenti MeshNumber C16.131.077.509 Laurence Moon Syndrome laurence moon syndrome MeshNumber C16.131.077.525 LEOPARD Syndrom ... more details
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