Recent advances in diagnosis, treatment, and outcome of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Reviews in Endocrine and Metabolic Disorders

Volumn 8, Issue 4, 2007, Pages 349-363

  Riepe, Felix G ^a   Sippell, Wolfgang G ^a  

^a UNIVERSITY OF KIEL   (Germany)

Author keywords

21 hydroxylase deficiency; Congenital adrenal hyperplasia; Fertility; Growth; Mortality; Newborn screening; Steroid detection

Indexed keywords

ANDROGEN; CORTICOSTEROID; DEXAMETHASONE; FLUDROCORTISONE; FLUTAMIDE; GLUCOCORTICOID; GONADORELIN AGONIST; GROWTH HORMONE; HYDROCORTISONE; MINERALOCORTICOID; STEROID 21 MONOOXYGENASE;

BODY HEIGHT; CONGENITAL ADRENAL HYPERPLASIA; DISEASE SEVERITY; DRUG DOSE REDUCTION; FERTILITY; GENDER IDENTITY; GENETICS; GROWTH; HORMONE METABOLISM; HUMAN; MASS SPECTROMETRY; MORBIDITY; MORTALITY; NEWBORN SCREENING; PATHOPHYSIOLOGY; PREDICTION; PRENATAL CARE; REVIEW; STEROID 21 MONOOXYGENASE DEFICIENCY; STEROID ANALYSIS; STRESS; TREATMENT OUTCOME;

ADRENAL HYPERPLASIA, CONGENITAL; HUMANS; HYDROCORTISONE; INFANT, NEWBORN; NEONATAL SCREENING; STEROID 21-HYDROXYLASE; TREATMENT OUTCOME;

EID: 38049048682     PISSN: 13899155     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11154-007-9053-1     Document Type: Review

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