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Titolo:
Congenital adrenal hyperplasias
Autore:
White, PC;
Indirizzi:
Univ Texas, SW Med Ctr, Div Pediat Endocrinol, Dallas, TX 75235 USA Univ Texas Dallas TX USA 75235 iv Pediat Endocrinol, Dallas, TX 75235 USA
Titolo Testata:
BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
fascicolo: 1, volume: 15, anno: 2001,
pagine: 17 - 41
SICI:
1521-690X(200103)15:1<17:CAH>2.0.ZU;2-P
Fonte:
ISI
Lingua:
ENG
Soggetto:
STEROID 21-HYDROXYLASE DEFICIENCY; BONE-MINERAL DENSITY; PLASMA-RENIN ACTIVITY; PRENATAL TREATMENT; ADULT HEIGHT; GENE; DIAGNOSIS; CHILDREN; GROWTH; SYSTEM;
Keywords:
steroid 21-monooxygenase; adrenal hyperplasia; congenital; cytochrome P-450; metabolism; inborn errors; sex differentiation disorders; virilism; hydrocortisone; aldosterone; androgens; HLA antigens;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Life Sciences
Citazioni:
90
Recensione:
Indirizzi per estratti:
Indirizzo: White, PC Univ Texas, SW Med Ctr, Div Pediat Endocrinol, 5323 Harry Hines Blvd, Dallas, TX 75235 USA Univ Texas 5323 Harry Hines Blvd Dallas TX USA 75235 X 75235 USA
Citazione:
P.C. White, "Congenital adrenal hyperplasias", BEST PRAC R, 15(1), 2001, pp. 17-41

Abstract

Congenital adrenal hyperplasia syndromes result from deficiencies of enzymes involved in corticosteroid biosynthesis. Most commonly, they are due to mutations in 21-hydroxylase. This chapter describes the clinical diagnosis and management of congenital adrenal hyperplasias throughout life, including in the fetus, child and adult. These clinical recommendations are explained in the context of the molecular and biochemical characteristics of the diseases.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/03/20 alle ore 23:17:24