Clinical and Biochemical Variability of Congenital Adrenal Hyperplasia Due to llβ-Hydroxylase Deficiency, A Study of 25 Patients

Journal of Clinical Endocrinology and Metabolism

Volumn 56, Issue 2, 1983, Pages 222-229

  Zachmann, Milo ^a   Tassinari, Davide ^a,b   Prader, Andrea ^a  

^a UNIVERSITY OF ZURICH   (Switzerland)

^b UNIVERSITY OF BOLOGNA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CORTISONE ACETATE; DEXAMETHASONE; OXYGENASE; TETRACOSACTIDE; TETRACOSACTIDE ZINC PHOSPHATE;

CARDIOVASCULAR SYSTEM; CHILD; CONGENITAL ADRENAL HYPERPLASIA; CONGENITAL DISORDER; CONGENITAL ENZYME DEFICIENCY; DRUG MONITORING; DRUG THERAPY; ENDOCRINE SYSTEM; ETHNIC OR RACIAL ASPECTS; HEREDITY; HERMAPHRODITISM; HUMAN; HYPERTENSION; INTRAMUSCULAR DRUG ADMINISTRATION; MAJOR CLINICAL STUDY; PSEUDOPRECOCIOUS PUBERTY; THERAPY;

17-KETOSTEROIDS; ADOLESCENT; ADRENAL HYPERPLASIA, CONGENITAL; ADULT; CHILD; CHILD, PRESCHOOL; CORTICOTROPIN; CORTODOXONE; FEMALE; HUMAN; HYDROCORTISONE; INFANT, NEWBORN; MALE; PREGNANEDIONES; PREGNANETRIOL; STEROID HYDROXYLASES; SUPPORT, NON-U.S. GOV'T;

EID: 0020698346     PISSN: 0021972X     EISSN: 19457197     Source Type: Journal    
DOI: 10.1210/jcem-56-2-222     Document Type: Article

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