An Extremely Rare <i>SRD5A2</i> Gene c.485A>C Mutation in a Compound Heterozygous Newborn with Disorders of Sex Development First Identified in Vietnam

<div>Patient’s abnormal genital phenotype: at the age of three days, (a) labia-majora-like bifid scrotum with clitoris-like microphallus and (b) perineoscrotal hypospadias; at the age of two years and three months, (c, d) microphallus had grown to 1.5 cm in length.</div>

Case Reports in Endocrinology

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Figure 1

Figure 1: An Extremely Rare <i>SRD5A2</i> Gene c.485A>C Mutation in a Compound Heterozygous Newborn with Disorders of Sex Development First Identified in Vietnam 

Figure 1 | An Extremely Rare SRD5A2 Gene c.485A>C Mutation in a Compound Heterozygous Newborn with Disorders of Sex Development First Identified in Vietnam 