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Results 1 - 10 of 18 for Hypotrichosis 5
  1. Autosomal recessive hypotrichosis 
    ... activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis. Hum Mutat. 2010 May;31(5):602-10. doi: 10.1002/humu.21235. Citation on PubMed
    https://medlineplus.gov/.../autosomal-recessive-hypotrichosis - Genetics
  2. LIPH gene 
    ... activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis. Hum Mutat. 2010 May;31(5):602-10. doi: 10.1002/humu.21235. Citation on PubMed Tanahashi K, Sugiura K, Takeichi T, Takama H, Shinkuma ... severity of hypotrichosis in adulthood. J Eur Acad Dermatol Venereol. 2013 ...
    https://medlineplus.gov/genetics/gene/liph - Genetics
  3. LPAR6 gene 
    ... receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3). Hum Genet. 2008 Jun;123(5):515-9. doi: 10.1007/s00439-008-0507- ... LIPH are associated with woolly hair and/or hypotrichosis. J Eur Acad Dermatol Venereol. 2013 May;27(5):545-9. doi: 10.1111/j.1468-3083. ...
    https://medlineplus.gov/genetics/gene/lpar6 - Genetics
  4. DSG4 gene 
    ... the desmoglein 4 gene underlies localized autosomal recessive hypotrichosis. J Invest Dermatol. 2005 Nov;125(5):1077-9. doi: 10.1111/j.0022-202X. ... 4 gene are associated with monilethrix-like congenital hypotrichosis. J Invest Dermatol. 2006 Jun;126(6):1281-5. doi: 10.1038/sj.jid.5700113. Citation on ...
    https://medlineplus.gov/genetics/gene/dsg4 - Genetics
  5. Nicolaides-Baraitser syndrome 
    ... P, Paradisi M. A rare cause of syndromic hypotrichosis: Nicolaides-Baraitser syndrome. J Am Acad Dermatol. 2008 Nov;59(5 Suppl):S92-8. doi: 10.1016/j.jaad. ...
    https://medlineplus.gov/.../condition/nicolaides-baraitser-syndrome - Genetics
  6. WNT10A gene 
    ... to sweat (hypohidrosis), sparse scalp and body hair (hypotrichosis), and several missing teeth (hypodontia) or teeth that are malformed. WNT10A gene mutations account for about 5 percent of all cases of hypohidrotic ectodermal dysplasia. ...
    https://medlineplus.gov/genetics/gene/wnt10a - Genetics
  7. Roberts syndrome 
    ... of the condition. Appelt-Gerken-Lenz syndrome Hypomelia hypotrichosis facial hemangioma syndrome Pseudothalidomide syndrome RBS Roberts-SC ... sister chromatid cohesion. Nat Genet. 2005 May;37(5):468-70. doi: 10.1038/ng1548. Epub 2005 ...
    https://medlineplus.gov/genetics/condition/roberts-syndrome - Genetics
  8. Is hair texture determined by genetics?: MedlinePlus Genetics 
    ... J Hum Genet. 2009 Aug;54(8):461-5. doi: 10.1038/jhg.2009.61. Epub 2009 ... Europeans. Am J Hum Genet. 2009 Nov;85(5):750-5. doi: 10.1016/j.ajhg.2009.10.009. ...
    https://medlineplus.gov/genetics/understanding/traits/hairtexture - Genetics
  9. RMRP gene 
    ... immune deficiency), elevated cancer risk, sparse hair growth (hypotrichosis), and other signs and symptoms of cartilage-hair ... a similar disorder known as metaphyseal dysplasia without hypotrichosis. This condition is characterized by short stature and ...
    https://medlineplus.gov/genetics/gene/rmrp - Genetics
  10. Monilethrix 
    ... People with monilethrix also have sparse hair growth (hypotrichosis) and short, brittle hair that breaks easily.Affected ... follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris. Cell. 2003 Apr 18; ...
    https://medlineplus.gov/genetics/condition/monilethrix - Genetics
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