Conocer la frecuencia de niños con hiperplasia suprarrenal congénita (HSC) en el hospital e .. sión tardía: observada en 30% de los casos, puede en-. Se usaron las palabas: hiperplasia adrenal congénita, déficit de 21 Ezquieta B. Hiperplasia suprarrenal congénita no clásica o tardía. Many translated example sentences containing “hiperplasia suprarrenal congénita” – English-Spanish dictionary and search engine for English translations.

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Am J Hum Genet, 37pp. Fertility and body composition after laparoscopic bilateral congrnita in a year old female with congenital adrenal hyperplasia. J Pediatr Surg, 27pp. Bone mineral density in relation to glucocorticoid substitution therapy in adult patients with hydroxylase deficiency. Structure-phenotype correlations of human CYP21A2 mutations in congenital adrenal hyperplasia.

Hiperplasia adrenal congénita por déficit de 21 hidroxilasa: un reto diagnóstico y terapéutico

Structural and functional analysis of a novel mutation of CYP21B in a heterozygote carrier of hydroxylase deficiency. Temporal and individual variations in the dose of glucocorticoid used for the treatment of salt-losing congenital virilizing adrenal hyperplasia due to hydroxylase deficiency.


Prenatal diagnosis and treatment of congenital adrenal hyperplasia.

J Pediatr Adolesc Gynecol. Klin Padiatr,pp. Bone density in young patients with congenital adrenal hyperplasia. Endocrinol Metab Clin North Am, 26pp. Neonatal screening for congenital adrenal hyperplasia. Persistent obesity and short final height after corticoid overtreatment for congenital adrenal hyperplasia CAH in infancy.

La diversidad del sistema endocrino. J Clin Invest, 90pp. High frequency of nonclassical steroid hydroxylase deficiency. The use of adrenalectomy as a treatment for congenital adrenal hyperplasia. An update on prenatal diagnosis and treatment of congenital adrenal hyperplasia. Mineralocorticoids in congenital adrenal hyperplasia. Acta Paediatr,pp. Psychoneuroendocrinology, 18pp.

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Increased prevalence of heterozygous OH germline mutations in patients with adrenal incidentalomas. Endocr Rev, 20pp. Tratado de endocrinologia pediatrica, pp. Acta Paediatr, 84pp. Comparison of one-tier and two-tier newborn screening metrics for congenital adrenal hyperplasia. Clin Endocrinol, 56pp. Clinical and molecular genetics of congenital adrenal hyperplasia due to suprarrebal deficiency.

Med Clin Barc, pp. Eur J Pediatr,pp. Aportaciones del analisis molecular en la hiperplasia suprarrenal congenita. Acta Paediatr, 89pp. Menstrual disturbance and hypersecretion of progesterone in women with congenital adrenal hyperplasia due to hydroxylase deficiency.

The effect on the fetal pituitary-adrenal axis of dexamethasone administration early in the second trimester of pregnancy.


Sistema OJS – Metabiblioteca. Endocr Rev, 15pp. Hiperplasia suparrenal congenita por defecto de la hidroxilasa. Trends Endocrinol Metab, 9pp. J Clin Endocrinol Metab, 74pp.

True precocious puberty complicating congenital adrenal hyperplasia: High prevalence of testicular adrenal rest tumors, impaired spermatogenesis and Leydig cell failure in adolescent and adult males with congenital adrenal hyperplasia. Tratado de endocrinologia pediatrica hipefplasia de la adolescencia.

J Clin Endocrinol Metab, 80pp. Congenital adrenal hyperplasia pearls you should know—globally. Genetic mapping of the hydroxylase deficiency gene within the HLA linkage group. Acta Paediatr Jpn, 30pp.


Endocrinol Metab Clin North Am, 30pp. Bone mineral density and body composition in congenital adrenal hiperplsaia. Long term outcome of classical hydroxylase deficiency: Indeed, a de novo RW mutation was found in patient 7.

Prenatal dexamethasone treatment of children at risk for congenital adrenal hyperplasia: