Tag Archives: 46 xy disorders

F1000 Commentary: Phenotypical, biological, and molecular heterogeneity of 5alpha-reductase deficiency: an extensive international experience of 55 patients

Posted on September 11, 2014 by

Maimoun L, Philibert P, Cammas B, Audran F, Servant N, Lubroso S, Paris F, Sultan C. J Clin Endocrinol Metab. 2011 Feb; 96:296-307 DOI: 10.1210/jc.2010-1024 Abstract CONTEXT: In 46,XY disorders of sex development, 5α-reductase deficiency is rare and is not usually … Continue reading →

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