Marie Unna congenital hypotrichosis

Common Name(s)

Marie Unna congenital hypotrichosis

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Marie Unna congenital hypotrichosis" for support, advocacy or research.

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General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Marie Unna congenital hypotrichosis" returned 1 free, full-text research articles on human participants. First 3 results:

Marie Unna congenital hypotrichosis: clinical description, histopathology, scanning electron microscopy of a previously unreported large pedigree.
 

Author(s): J L Roberts, D A Whiting, D Henry, G Basler, L Woolf

Journal: J. Investig. Dermatol. Symp. Proc.. 1999 Dec;4(3):261-7.

 

Marie Unna congenital hypotrichosis (MUCH) is a rare autosomal dominant condition in which abnormalities are confined to hair shaft structure and hair density. We report a six-generation pedigree consisting of 59 members of whom 16 are affected; nine identified affected individuals ...

Last Updated: 14 Mar 2000

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The terms "Marie Unna congenital hypotrichosis" returned 0 free, full-text review articles on human participants.

 
 
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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

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