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A novel splice site variant in CYP11A1 in trans with the p.E314K variant in a male patient with congenital adrenal insufficiency

机译:男性先天性肾上腺功能不全患者中CYP11A1的新剪接位点变异与p.E314K变异

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摘要

BackgroundThe CYP11A1 gene encodes the cytochrome P450 side‐chain cleavage enzyme, which is essential for steroid formation. Recessive variants in this gene can lead to impairment of sexual differentiation caused by a complete or partial loss of steroid hormone production. The phenotypic spectrum in affected 46XY males may vary from surgically repairable defects including cryptorchidism and hypospadias to complete feminization of external gonads, accompanied by symptoms of adrenal dysfunction.
机译:背景CYP11A1基因编码细胞色素P450侧链裂解酶,这对于类固醇形成至关重要。该基因的隐性变异可导致类固醇激素产生完全或部分丧失,从而导致性分化受损。受影响的46XY男性的表型谱可能有所不同,从可手术修复的缺陷(包括隐睾症和尿道下裂)到外部性腺完全女性化,并伴有肾上腺功能障碍的症状。

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