Molecular characterization of 6 unrelated Italian patients with 5alpha-reductase type 2 deficiency

• Published in: Journal of andrology Vol. 29; no. 1; p. 20
• Main Authors: Baldinotti, F, Majore, S, Fogli, A, Marrocco, G, Ghirri, P, Vuerich, M, Tumini, S, Boscherini, B, Vetri, M, Scommegna, S, Rinaldi, R, Simi, P, Grammatico, P
• Format: Journal Article
• Language: English
• Published: United States 01.01.2008
• Subjects: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase - deficiency; 3-Oxo-5-alpha-Steroid 4-Dehydrogenase - genetics; Adolescent; Adult; Child; Codon, Nonsense; Dihydrotestosterone - metabolism; Disorders of Sex Development - genetics; Disorders of Sex Development - pathology; Female; Heterozygote; Humans; Hypospadias - genetics; Hypospadias - pathology; Infant, Newborn; Italy; Male; Mutation, Missense; Polymorphism, Genetic; Sex Differentiation - genetics; Italy
• ISSN: 0196-3635
• DOI: 10.2164/jandrol.107.002592

Steroid 5alpha-reductase (5alphaR) deficiency (OMIM number #264600) is a rare 46,XY disorder of sex differentiation caused by mutations in the 5alphaR type 2 gene (SRD5A2) resulting in dihydrotestosterone deficiency during fetal development. We report on the analysis of the SRD5A2 gene in 6 unrelated 46,XY Italian patients with external genitalia morphology ranging from predominantly female to nearly completely male. Three subjects were seen and assessed at birth, 1 patient was referred to us before puberty, and 2 at postpubertal age. Six different causative mutations (5 missense and 1 nonsense) and a rare polymorphism were identified. Four patients presented homozygous single-base substitutions. These SRD5A2 mutations were located in exon 2 (variant Cys133Gly), exon 4 (Gly196Ser and Ala207Asp) and exon 5 (Tyr235Phe). A fifth subject was a compound heterozygote who carried a nonsense mutation in exon 1 (Trp53X) and a second SRD5A2 alteration in exon 5 (Tyr235Phe). The final patient presented a mutation in only 1 allele (Gly34Trp) together with the Ala49Thr variant. The molecular characterization of these patients made it possible to identify novel mutations and to confirm, before gender assignment or any surgical approach, the suspected 5alphaR deficiency in 2 newborns, 1 of whom had inconclusive hormonal data. 5alphaR deficiency in subjects without parental consanguinity and the presence of compound heterozygotic patients suggest that SRD5A2 mutations carrier frequency may be higher than previously thought.