21-Hydroxylase deficiency: Clinical features, laboratory profile and pointers to diagnosis in Indian children

Indian Pediatrics

Volumn 41, Issue 12, 2004, Pages 1226-1232

  Bajpai, Anurag ^a   Kabra, Madhulika ^a   Menon, P S N ^a  

^a ALL INDIA INSTITUTE OF MEDICAL SCIENCES   (India)

Author keywords

21 hydroxylase deficiency; Ambiguous genitalia; Congenital adrenal hyperplasia

Indexed keywords

BICARBONATE; CREATININE; HYDROXYPROGESTERONE; POTASSIUM; PRASTERONE; SODIUM; STEROID 21 MONOOXYGENASE; TESTOSTERONE; UREA;

ANAMNESIS; ANDROGEN BLOOD LEVEL; ARTICLE; BICARBONATE BLOOD LEVEL; BLOOD PH; CLINICAL FEATURE; CORTICOTROPIN BLOOD LEVEL; CORTICOTROPIN TEST; CREATININE BLOOD LEVEL; CRYPTORCHISM; ECHOGRAPHY; FEMALE; FEMALE PSEUDOHERMAPHRODITISM; HUMAN; KARYOTYPE 46,XX; MAJOR CLINICAL STUDY; MALE; POTASSIUM BLOOD LEVEL; SALT LOSING NEPHRITIS; SODIUM BLOOD LEVEL; STEROID 21 MONOOXYGENASE DEFICIENCY; TESTOSTERONE BLOOD LEVEL; UREA BLOOD LEVEL; VIRILIZATION;

ADRENAL HYPERPLASIA, CONGENITAL; FEMALE; GENITALIA; HUMANS; INDIA; INFANT; INFANT, NEWBORN; MALE; NEONATAL SCREENING;

EID: 11944249874     PISSN: 00196061     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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