Title : Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase Deficiency.

Pub. Date : 2020

PMID : 33780934






1 Functional Relationships(s)
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1 CONTEXT: Steroid 17alpha-hydroxylase/17,20-lyase deficiency (17OHD) is characterized by decreased sex steroids and cortisol, and excessive mineralocorticoid action. Steroids cytochrome P450 family 17 subfamily A member 1 Homo sapiens