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Hypotrichosis 3
- ... lipase H gene underlie autosomal recessive woolly hair/hypotrichosis. J Invest Dermatol. 2009 Mar;129(3):622-8. doi: 10.1038/jid.2008.290. ...
- ... follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris. Cell. 2003 Apr 18;113(2):249-60. doi: 10.1016/s0092-8674(03)00273-3. Citation on PubMed Korge BP, Hamm H, Jury ...
- ... ribonucleoprotein assembly. Biochim Biophys Acta. 2008 Mar;1783(3):455-66. doi: 10.1016/j.bbamcr.2007.11.016. Epub 2007 Dec 8. Citation on PubMed
- ... hair syndrome Comel-Netherton syndrome Ichthyosiform erythroderma with hypotrichosis and hyper-IgE Ichthyosis linearis circumflexa ILC NETH ... intronic mutations. J Invest Dermatol. 2012 Mar;132(3 Pt 1):575-82. doi: 10.1038/jid. ...
- ... features of oculodentodigital dysplasia include sparse hair growth (hypotrichosis), brittle nails, an unusual curvature of the fingers ( ... dysplasia: study of ophthalmological and clinical manifestations in three boys with probably autosomal recessive inheritance. Ophthalmic Genet. ...
- ... tend to have sparse scalp and body hair (hypotrichosis). EDA-ID is also characterized by missing teeth ( ... recognition and diagnosis. Arch Dermatol. 2008 Mar;144(3):342-6. doi: 10.1001/archderm.144.3. ...
- ... P, Paradisi M. A rare cause of syndromic hypotrichosis: Nicolaides-Baraitser syndrome. J Am Acad Dermatol. 2008 ... Genet C Semin Med Genet. 2014 Sep;166C(3):302-14. doi: 10.1002/ajmg.c.31409. ...
- ... tend to have sparse scalp and body hair (hypotrichosis). The hair is often light-colored, brittle, and ... and sweat glands. Mutations in any of these three genes lead to the major signs and symptoms ...
- ... on their scalp where hair does not grow (hypotrichosis). About half of people with CIPA show signs ... nervous system. Curr Opin Neurobiol. 2000 Jun;10(3):381-91. doi: 10.1016/s0959-4388(00) ...