17 alpha-hydroxylase deficiency classification

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mehrian Jafarizade, M.D [2]

Overview

17 alpha-hydroxylase deficiency may be classified into two types, based on clinical findings: partial form and severe form.

Classification

17 alpha-hydroxylase deficiency may be classified into two types, based on clinical findings severity: partial form and severe form.[1]

Reference

  1. Kater CE, Biglieri EG (1994). "Disorders of steroid 17 alpha-hydroxylase deficiency". Endocrinol. Metab. Clin. North Am. 23 (2): 341–57. PMID 8070426.