Braun-Bayer syndrome: Difference between revisions
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Created page with "__NOTOC__ {{SI}} {{CMG}} {{SK}} Nephrosis - deafness - urinary tract - digital malformations ==Overview== Braun-Bayer syndrome is characterized by anomalies of the urinary tra..." |
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{{SK}} Nephrosis - deafness - urinary tract - digital malformations | {{SK}} Nephrosis - deafness - urinary tract - digital malformations | ||
==Overview== | ==Overview== |
Latest revision as of 20:15, 9 October 2012
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Nephrosis - deafness - urinary tract - digital malformations
Overview
Braun-Bayer syndrome is characterized by anomalies of the urinary tract, thumbs and big toes, deafness and nephrosis. It has been described in five brothers. The mode of transmission has not been clearly established but seems to be either autosomal recessive or X-linked dominant.