We report on seven Iraqi patients with 46,XY karyotype and ambiguous genitalia characterized by perineo-scrotal hypospadias, bifid scrotum, clitoris like phallus, palpable testes in inguinal canal and pseudovagina. Patients were raised five as females and two as males. They are all unrelated with the exception of two couples of brothers. The diagnosis of 5-α-reductase-2 deficiency syndromewas first hypothesized on clinical grounds and then confirmed by molecular analysis. Direct sequencing analysis of the SRD5A2 gene revealed in five patients a novel homozygous frame-shiftmutation (c.453delC) and in two related patients a previous reportedmissensemutation. The presence of the same mutation in unrelated patients of the same population suggests a possible founder effect. This report brings the 5-α-reductase-2 deficiency syndrome to the attention of clinical geneticists and child surgeons and discusses the appropriate clinical and surgical strategies for treating these patients.

Di Marco, C., Bulotta, A.L., Varetti, C., Dosa, L., Michelucci, A., Baldinotti, F., et al. (2013). Ambiguous external genitalia due to defect of 5-α-reductase in seven Iraqi patients: Prevalence of a novel mutation. GENE, 526(7), 490-493 [10.1016/j.gene.2013.04.070].

Ambiguous external genitalia due to defect of 5-α-reductase in seven Iraqi patients: Prevalence of a novel mutation

BULOTTA, ANNA LAVINIA;VARETTI, CONCETTA;DOSA, LAURA;CASTAGNINI, CINZIA;MARI, FRANCESCA;RENIERI, ALESSANDRA;MESSINA, MARIO
2013

Abstract

We report on seven Iraqi patients with 46,XY karyotype and ambiguous genitalia characterized by perineo-scrotal hypospadias, bifid scrotum, clitoris like phallus, palpable testes in inguinal canal and pseudovagina. Patients were raised five as females and two as males. They are all unrelated with the exception of two couples of brothers. The diagnosis of 5-α-reductase-2 deficiency syndromewas first hypothesized on clinical grounds and then confirmed by molecular analysis. Direct sequencing analysis of the SRD5A2 gene revealed in five patients a novel homozygous frame-shiftmutation (c.453delC) and in two related patients a previous reportedmissensemutation. The presence of the same mutation in unrelated patients of the same population suggests a possible founder effect. This report brings the 5-α-reductase-2 deficiency syndrome to the attention of clinical geneticists and child surgeons and discusses the appropriate clinical and surgical strategies for treating these patients.
Di Marco, C., Bulotta, A.L., Varetti, C., Dosa, L., Michelucci, A., Baldinotti, F., et al. (2013). Ambiguous external genitalia due to defect of 5-α-reductase in seven Iraqi patients: Prevalence of a novel mutation. GENE, 526(7), 490-493 [10.1016/j.gene.2013.04.070].
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11365/973610