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Results 1 - 9 of 9 for Hypotrichosis 4
  1. ... Orlow SJ, Christiano AM. Mutations in the desmoglein 4 gene underlie localized autosomal recessive hypotrichosis with monilethrix hairs and congenital scalp erosions. J ...
  2. ... RJ, Panteleyev AA, Nguyen VT, Christiano AM. Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris. Cell. 2003 Apr 18; ...
  3. ... of the condition. Appelt-Gerken-Lenz syndrome Hypomelia hypotrichosis facial hemangioma syndrome Pseudothalidomide syndrome RBS Roberts-SC ... 1007/s00412-006-0072-6. Epub 2006 Jul 4. Citation on PubMed or Free article on PubMed ...
  4. ... hair syndrome Comel-Netherton syndrome Ichthyosiform erythroderma with hypotrichosis and hyper-IgE Ichthyosis linearis circumflexa ILC NETH ... health. Int J Cosmet Sci. 2009 Aug;31(4):247-54. doi: 10.1111/j.1468-2494. ...
  5. ... on their scalp where hair does not grow (hypotrichosis). About half of people with CIPA show signs ... type IV Hereditary sensory and autonomic neuropathy, type 4 HSAN type IV HSAN4 Genetic Testing Registry: Hereditary ...
  6. ... features of oculodentodigital dysplasia include sparse hair growth (hypotrichosis), brittle nails, an unusual curvature of the fingers ( ... Eur J Med Genet. 2005 Oct-Dec;48(4):377-87. doi: 10.1016/j.ejmg.2005. ...
  7. ... tend to have sparse scalp and body hair (hypotrichosis). The hair is often light-colored, brittle, and ... A, Bonnefont JP, Bodemer C, Smahi A. Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for ...
  8. ... P, Paradisi M. A rare cause of syndromic hypotrichosis: Nicolaides-Baraitser syndrome. J Am Acad Dermatol. 2008 ... Baraitser syndrome. Nat Genet. 2012 Feb 26;44(4):445-9, S1. doi: 10.1038/ng.1105. ...
  9. ... tend to have sparse scalp and body hair (hypotrichosis). EDA-ID is also characterized by missing teeth ( ... of NEMO protein. Blood. 2011 Jul 28;118(4):926-35. doi: 10.1182/blood-2010-10- ...