Practical approach to steroid 5alpha-reductase type 2 deficiency
- نوع فایل : کتاب
- زبان : انگلیسی
- مؤلف : Chong Kun Cheon
- چاپ و سال / کشور: 2011
Description
The aim of this article is to review the literature on steroid 5alpha-reductase type 2 deficiency (5ل-RD2) to provide clinicians with information to guide their management of patients with this disorder. The 5alpha-reductase type 2 is encoded by the 5alpha-reductase type 2 gene (SRD5A2) on chromosome 2 and is predominantly expressed in external genital tissues and the prostate. Mutations of the SRD5A2 gene leads to an uncommon autosomal recessive disorder affecting sexual differentiation in individuals with 46,XY karyotype; their phenotype can range from almost normal female structures to a distinct male phenotype with ambiguous genitalia at birth. These phenotypes result from impaired conversion of testosterone to dihydrotestosterone due to mutations in the SRD5A2 gene. Patients exhibit virilization at puberty without breast development, which is often accompanied by gender identity change from female to male. More than 40 mutations have been reported in all five exons of the SRD5A2 gene. Phenotype–genotype correlations for 5ل-RD2 have not been well established. The newborn phenotypes of male pseudohermaphrodites with 5ل-RD2, partial androgen insensitivity syndrome (PAIS), or 17â-hydroxysteroid dehydrogenase type 3 (17â-HSD3) enzyme deficiency may be indistinguishable. We conclude that steroid 5ل-RD2 should be included in the differential diagnosis of newborns with 46,XY DSD. It is important that the diagnosis be made in infancy by biochemical and molecular studies before gender assignment or any surgical intervention because these patients should be considered males at birt
Eur J Pediatr (2011) 170:1–8 Received: 25 February 2010 / Accepted: 9 March 2010 / Published online: 28 March 2010
