HIGHLIGHTS
- who: HLA-DRB et al. from the Department of Endocrinology, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China, Department of have published the research: Clinical and Genetic Analysis of a Patient With Coexisting 17a-Hydroxylase/17,20-Lyase De ciency and Moyamoya Disease, in the Journal: (JOURNAL)
SUMMARY
17a-Hydroxylase/17,20-lyase (17OHD) deficiency (OMIM 202110) is a rare form of congenital adrenal hyperplasia (CAH). It is an autosomal recessive disease caused by a gene defect in cytochrome P450 family 17 subfamily A member 1 (CYP17A1). The full length of . . .
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