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Results 1 - 8 of 8 for Hypotrichosis 2
  1. ... 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) ...
  2. ... lipase H gene underlie autosomal recessive woolly hair/hypotrichosis. J Invest Dermatol. 2009 Mar;129(3):622-8. doi: 10.1038/jid.2008.290. Epub 2008 Oct 2. Citation on PubMed Shimomura Y. Congenital hair loss ...
  3. ... of the condition. Appelt-Gerken-Lenz syndrome Hypomelia hypotrichosis facial hemangioma syndrome Pseudothalidomide syndrome RBS Roberts-SC ... 14. Citation on PubMed Hou F, Zou H. Two human orthologues of Eco1/Ctf7 acetyltransferases are both ...
  4. ... hair syndrome Comel-Netherton syndrome Ichthyosiform erythroderma with hypotrichosis and hyper-IgE Ichthyosis linearis circumflexa ILC NETH ... 21 families. J Invest Dermatol. 2002 Feb;118(2):352-61. doi: 10.1046/j.1523-1747. ...
  5. ... on their scalp where hair does not grow (hypotrichosis). About half of people with CIPA show signs ... and autonomic neuropathies. Neurobiol Dis. 2006 Feb;21(2):247-55. doi: 10.1016/j.nbd.2005. ...
  6. ... features of oculodentodigital dysplasia include sparse hair growth (hypotrichosis); brittle nails; and a skin condition called palmoplantar ... with normal cell growth and cell specialization. These two processes determine the shape and function of many ...
  7. ... tend to have sparse scalp and body hair (hypotrichosis). EDA-ID is also characterized by missing teeth ( ... inflammatory bowel disease or rheumatoid arthritis.There are two forms of EDA-ID that have similar signs ...
  8. ... tend to have sparse scalp and body hair (hypotrichosis). The hair is often light-colored, brittle, and ... pathway that is critical for the interaction between two cell layers, the ectoderm and the mesoderm. In ...