Se usaron las palabas: hiperplasia adrenal congénita, déficit de 21 Alonso M, Ezquieta B. Hiperplasia suprarrenal congénita no clásica o. Download Citation on ResearchGate | On Aug 6, , B. Cánovas Gaillemin and others published Hiperplasia suprarrenal congénita }. Request PDF on ResearchGate | On Jan 31, , B. Huidobro Fernández and others published Consejo genético en la hiperplasia suprarrenal congénita por.

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Adrenal hydroxylase deficiency in childhood: Acta Pediatr Esp, 59pp. Endocrinol Metab Clin North Am, 30pp. The pathophysiology and genetics of congenital lipoid adrenal hyperplasia.

Pediatr Res, 33pp. Increased bone mineral density in congenital adrenal hyperplasia CAH. Children with classic congenital adrenal hyperplasia have elevated serum leptin concentrations and insulin resistance: N Engl J Med.

An Pediatr, 58pp. Genotype-phenotype correlation in 1, families with congenital adrenal hyperplasia owing to hydroxylase deficiency. Los varones enfermos no presentan signos aparentes en los genitales externos y se detectan al producirse la crisis adrenal.


Over the long-term course of the disease, these patients can develop a series of complications that include short stature, obesity, reduced bone mineral density, gonadal dysfunction, infertility and psychosexual dysfunction in women.

Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to hydroxylase deficiency. J Pediatr Surg, 27pp. Randomised controlled trial of growth effect of hydrocortisone in congenital adrenal hyperplasia. Hum Genet, 96pp. Response to treatment of congenital adrenal hyperplasia in infancy.

Menstrual disturbance and hypersecretion of progesterone congeniya women with congenital adrenal hyperplasia due to hydroxylase deficiency. Trends Endocrinol Metab, 9pp. J Pediatr Adolesc Gynecol.

Hiperplasia suprarrenal congenita estudiaron 9 pacientes diagnosticados en la etapa perinatal y 8 durante la etapa pre y postpuberal. Acta Endocrinol,pp. J Ckasica Endocrinol Metab, 81pp.

Disease expression and molecular genotype in congenital adrenal hyperplasia due to hydroxylase deficiency. J Clin Endocrinol Metab, 74pp.

Prenatal diagnosis and treatment of congenital adrenal hyperplasia. Horm Res,pp.

Growth of patients with hydroxylase deficiency: Int J Pediatr Endocrinol. Personality characteristics and platelet MAO activity in women with congenital adrenal hyperplasia. Adv Hum Gen, 20pp. New ideas for medical treatment of congenital adrenal hyperplasia. J Clin Endocrinol Metab. Tratado de endocrinologia pediatrica, pp. J Clin Endocrinol Metab, 79pp. An update on prenatal diagnosis and treatment of congenital adrenal hiper;lasia. Trends Endocrinol Metab, 9pp.


Arch Dis Child, 65pp. Bilateral laparoscopic adrenalectomy as a treatment for classic congenital adrenal hyperplasia attributable to hydroxylase deficiency abstract.


The role of androgens in male gender role behaviour. Lancet,pp. Psychosexual outcome of assigned females and males with 46,XX virilizing congenital adrenal hyperplasia.

High frequency of nonclassical steroid hydroxylase deficiency. Pediatr Clin North Am. J Pediatr Surg, 29pp.


Long term outcome of classical hydroxylase deficiency: J Clin Invest, 90pp. La diversidad del sistema endocrino. Clin Endocrinol Oxf21pp.