CYP11A1 Mutations Result in Various Clinical Phenotypes
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Poster Presentations
P: 2-3
June 2017

CYP11A1 Mutations Result in Various Clinical Phenotypes

1. Göztepe Training And Research Hospital, Clinic Of Pediatrics, Istanbul, Turkey
2. Amasya University Faculty Of Medicine, Department Of Pediatrics, Amasya, Turkey
3. Birmingham University, London, Uk
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Cytochrome P450 side-chain cleavage enzyme (CYP11A1) is the first enzyme and catalyzes the rate-limiting step of steroidogenesis. CYP11A1 deficiency is associated with adrenal insufficiency (AI) and commonly with a disorder of sex development (DSD) in 46,XY individuals. Our objective was to define the clinical presentation of our patients with CYP11A1 mutations, one of whom had a novel CYP11A1 mutation.

Four patients were presented. Case 2 has been reared as a girl and she has a novel CYP11A1 mutation. Cases 3 and 4 are siblings. Clinical findings are given in Table 1.

These cases demonstrate that CYP11A1 deficiency can be seen in the newborn period or in early childhood as classical or non-classical forms. Normal genital appearance can found in 46,XY patients in non-classic form and this does not exclude life-threatening AI risk.