Combined 21-hydroxylase and 11β-hydroxylase deficiency: Patient report and molecular basis

Journal of Pediatric Endocrinology and Metabolism

Volumn 13, Issue 7, 2000, Pages 945-949

  Gillis, D ^a   Speiser, P ^a   Zhou, Z ^a   Rosler, A ^a  

^a HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

Author keywords

11 hydroxylase deficiency; 21 hydroxylase deficiency; Congenital adrenal hyperplasia; CYP11 1; CYP21; Salt wasting

Indexed keywords

STEROID 11BETA MONOOXYGENASE;

ARTICLE; CASE REPORT; CONGENITAL ADRENAL HYPERPLASIA; DISEASE ASSOCIATION; ELECTROLYTE DISTURBANCE; ENZYME DEFICIENCY; FEMALE; GENE MUTATION; GENE STRUCTURE; HUMAN; INTRON; NEWBORN; SALT LOSING NEPHRITIS; STEROID 21 MONOOXYGENASE DEFICIENCY;

ADRENAL HYPERPLASIA, CONGENITAL; BASE SEQUENCE; DNA PRIMERS; FEMALE; HUMANS; INFANT, NEWBORN; MUTATION; POLYMERASE CHAIN REACTION; STEROID 11-BETA-HYDROXYLASE; STEROID 21-HYDROXYLASE;

EID: 0033864153     PISSN: 0334018X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (22)

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3. Secondary biosynthetic defects in women with late-onset congenital adrenal hyperplasia
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17. Testosterone-induced hypertension in the rat
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