These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Search MEDLINE/PubMed
Title: Marie Unna hereditary hypotrichosis. Author: Argenziano G, Sammarco E, Rossi A, Delfino M, Calvieri S. Journal: Eur J Dermatol; 1999 Jun; 9(4):278-80. PubMed ID: 10356404. Abstract: Hereditary congenital hypotrichosis is an autosomal dominant pilar dysplasia first described by Marie Unna in an extended German family. The diffuse hair defect typically occurs as an isolated phenomenon and the ultrastructural hair findings consist of both torsion and longitudinal grooving of the hair shaft. A large pedigree comprising 6 generations with 20 members affected by Marie Unna hypotrichosis from Italy is reported.[Abstract] [Full Text] [Related] [New Search]