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

Search MEDLINE/PubMed


  • Title: Marie-Unna hereditary hypotrichosis: case report and review of the literature.
    Author: Podjasek JO, Hand JL.
    Journal: Pediatr Dermatol; 2011; 28(2):202-4. PubMed ID: 21504454.
    Abstract:
    We present an 18-year-old girl with progressively worsening hair thinning and loss since puberty. Her clinical history, physical examination, and pathology results were consistent with Marie-Unna hereditary hypotrichosis, a rare cause of autosomal dominant hereditary hair loss. She had no family history of similar hair loss and represents the first report of a new case of Marie-Unna hereditary hypotrichosis within a previously unaffected family.
    [Abstract] [Full Text] [Related] [New Search]