| Marie-Unna hereditary hypotrichosis: case report and review of the literature. | |
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MedLine Citation:
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PMID: 21504454 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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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. |
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Authors:
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Joshua O Podjasek; Jennifer L Hand |
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Publication Detail:
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Type: Case Reports; Journal Article; Review |
Journal Detail:
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Title: Pediatric dermatology Volume: 28 ISSN: 1525-1470 ISO Abbreviation: Pediatr Dermatol Publication Date: 2011 Mar-Apr |
Date Detail:
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Created Date: 2011-04-20 Completed Date: 2011-08-18 Revised Date: 2011-12-21 |
Medline Journal Info:
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Nlm Unique ID: 8406799 Medline TA: Pediatr Dermatol Country: United States |
Other Details:
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Languages: eng Pagination: 202-4 Citation Subset: IM |
Copyright Information:
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© 2011 Wiley Periodicals, Inc. |
Affiliation:
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Department of Dermatology, Mayo Clinic, Rochester, Minnesota 55905, USA. |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Adolescent Female Hair / abnormalities*, ultrastructure* Humans Hypotrichosis / congenital, pathology Microscopy, Electron |
| Comments/Corrections | |
Comment In:
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Pediatr Dermatol. 2011 Nov-Dec;28(6):750-1; author reply 751-2
[PMID:
22082473
]
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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