The earlier described mutation (c.307C > T [p.R103X]) in the SRD5A2 gene causing a 46,XY female phenotype

ŞİMŞEK E., Binay C., Ceylaner S.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, vol.25, pp.543-545, 2012 (SCI-Expanded) identifier identifier identifier


Deletions and mutations in the 5-alpha-reductase type 2 (SRD5A2) gene have been identified in 46,XY disorders of sexual differentiation (DSD). The clinical spectrum is heterogeneous, varying from a normal female external genital appearance to clitoromegaly and isolated micropenis or microphallus associated with hypospadias of various degrees. We describe a 46, XY DSD patient with a homozygous c.307C>T (p.R103X) mutation in the SRD5A2 gene. The case presented with a normal female external genital phenotype.