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Hypotrichosis 13
- ... Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families. Br J Dermatol. 2009 May;160( ...
- ... mutations develop monilethrix and others develop autosomal recessive hypotrichosis (described above). These conditions may represent different forms of the same disorder. More About This Health Condition cadherin family member 13 CDGF13 CDH family member 13 CDHF13 desmoglein-4 ...
- ... of the condition. Appelt-Gerken-Lenz syndrome Hypomelia hypotrichosis facial hemangioma syndrome Pseudothalidomide syndrome RBS Roberts-SC ... human syndromes. Chromosoma. 2007 Feb;116(1):1-13. doi: 10.1007/s00412-006-0072-6. Epub ...
- ... hair syndrome Comel-Netherton syndrome Ichthyosiform erythroderma with hypotrichosis and hyper-IgE Ichthyosis linearis circumflexa ILC NETH ... 1468-2494.2009.00516.x. Epub 2009 May 13. Citation on PubMed Sprecher E, Chavanas S, DiGiovanna ...
- ... on their scalp where hair does not grow (hypotrichosis). About half of people with CIPA show signs ... to pain with anhidrosis. Nat Genet. 1996 Aug;13(4):485-8. doi: 10.1038/ng0896-485. ...