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Results 1 - 9 of 9 for Hypotrichosis 3
  1. ... lipase H gene underlie autosomal recessive woolly hair/hypotrichosis. J Invest Dermatol. 2009 Mar;129(3):622-8. doi: 10.1038/jid.2008.290. ...
  2. ... 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 ...
  3. ... 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
  4. ... 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. ...
  5. ... 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. ...
  6. ... 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. ...
  7. ... 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. ...
  8. ... 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 ...
  9. ... 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) ...