Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
17-beta-hydroxysteroid dehydrogenase deficiency genotyping
Introduction
Overview
Overview
17 beta hydroxysteroid dehydrogenase deficiency is a condition with genotypically male and phenotypically female characteristics. There has been no phenotype to genotype correlation.
Genotyping
Genotyping
- 17 beta hydroxysteroid dehydrogenase deficiency is a condition with genotypically male and phenotypically female characterstics. There has been no phenotype to genotype correlation.[1]
References
References
- ↑ George MM, New MI, Ten S, Sultan C, Bhangoo A (2010). “The clinical and molecular heterogeneity of 17βHSD-3 enzyme deficiency”. Horm Res Paediatr. 74 (4): 229–40. doi:10.1159/000318004. PMID 20689261.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Abdulkerim Yassin, M.B.B.S[2]