Genetic aspects of congenital adrenal hyperplasia

Journal of Pediatric Endocrinology and Metabolism

Volumn 14, Issue SUPPL. 5, 2001, Pages 1303-1308

  Dacou Voutetakis, C ^a   Miniati Christidi, M ^a   Dracopoulou Vabouli, M ^a  

^a UNIVERSITY OF ATHENS MEDICAL SCHOOL   (Greece)

Author keywords

Congenital adrenal hyperplasia; CYP11B1 mutations; CYP17 mutations; CYP21 mutations; HSD3 1 mutations; HSD32b2 mutations; StAR gene mutations

Indexed keywords

3(OR 17)BETA HYDROXYSTEROID DEHYDROGENASE; CHOLESTEROL; HYDROXYSTEROID DEHYDROGENASE; ISOENZYME; STEROID 11BETA MONOOXYGENASE; STEROID 17ALPHA MONOOXYGENASE; STEROID 21 MONOOXYGENASE; STEROIDOGENIC ACUTE REGULATORY PROTEIN;

ADRENAL GLAND; ADRENAL INSUFFICIENCY; ARTICLE; CHILD; CLINICAL FEATURE; CONGENITAL ADRENAL HYPERPLASIA; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; FEMALE; FEMALE GENITAL SYSTEM; GENE DELETION; GENE MUTATION; GENETIC CODE; GENOTYPE; GONAD; HETEROZYGOSITY; HORMONE DEFICIENCY; HUMAN; HYPERTENSION; HYPOGONADISM; KARYOTYPE 46,XY; MALE; MITOCHONDRIAL MEMBRANE; PHENOTYPE; PRECOCIOUS PUBERTY; SEX DIFFERENTIATION; SEXUAL MATURATION; STEROIDOGENESIS; VIRILIZATION;

ADRENAL HYPERPLASIA, CONGENITAL; GENE FREQUENCY; GREECE; HUMANS; PHOSPHOPROTEINS; STEROID HYDROXYLASES;

EID: 0035178310     PISSN: 0334018X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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