Hiperplasia suprarrenal congénita variedad perdedora de sal. Presentación de un caso clínico. Congenital adrenal hyperplasia salt. Objetivo. Conocer la frecuencia de niños con hiperplasia suprarrenal congénita ( HSC) en el hospital e identificar las manifestacio- nes clínicas a su ingreso. Entradas sobre Hiperplasia Suprarrenal Congénita escritas por Laura Inter.

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Two genes encoding steroid hydroxylase are located near the genes encoding the fourth component of complement in man.

Non-classical hydroxylase deficiency suprsrrenal infancy and childhood: To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.

Bone, 18pp. Treatment and disease effects on short-term growth and adult height in children and adolescents with hydroxylase deficiency.

Adv Hum Gen, 20pp. Ovarian steroidogenesis in an adrenalectomized girl with hydroxylase deficiency.

Arch Dis Child, 78pp. Increased prevalence of heterozygous OH germline mutations in patients with adrenal incidentalomas.

Behavioral Neuroscience, 1 Previous article Next article. Prenatal treatment of congenital adrenal hyperplasia resulting from hydroxylase deficiency.


Clinical and molecular genetics of congenital adrenal hyperplasia due to hydroxylase deficiency. Nonisotopic detection of point mutations in the CYP21B gene in hydroxylase deficiency. Clinical Endocrinology72 4 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.

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View All Subscription Options. Analysis of steroid hydroxylase gene in the Spanish population. J Pediatr Surg, 27pp. Bone mineral density in relation to glucocorticoid substitution therapy in adult patients with hydroxylase deficiency.

Congenital adrenal hyperplasia is a term that includes all hereditary disorders of adrenal cortisol synthesis. Full text is only aviable in PDF. Eur J Endocrinol,pp. Growth and body proportions in congenital adrenal hyperplasia. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. Adrenal incidentaloma and patients with homozygous or heterozygous congenital adrenal hyperplasia. J Clin Endocrinol Metab, 84pp. An Pediatr, 58pp.

Congenital adrenal hyperplasia hhiperplasia to hydroxylase deficiency. Bone density in young patients with congenital adrenal hyperplasia. Prenatal diagnosis and treatment of congenital adrenal hyperplasia. Prenatal hormones and childhood sex segregation: Proceedings of the National Academy of Sciences, 7Horm Res, 58pp.


Flutamide, testolactone, and reduced hydrocortisone dose maintain normal growth velocity and bone maturation despite elevated androgen levels in children with congenital adrenal hyperplasia. Arch Dis Child, 65pp. Endocr Rev, 20pp. Investigaciones sobre la salud.

Hiperplasia suprarrenal congénita (CAH por sus siglas en inglés): Artículos científicos

Randomised controlled trial of growth effect of hydrocortisone in congenital adrenal hyperplasia. Clin Endocrinol, 56pp. Comprehensive genetic analysis of unrelated families with congenital adrenal hyperplasia due to hydroxylase deficiency. Arch Pediatr, 1pp. Turn off more accessible mode.

HIPERPLASIA SUPRARRENAL CONGÉNITA | Tratado de endocrinología pediátrica, 4e | McGraw-Hill Medical

Adrenarche does not occur in treated patients with congenital adrenal hyperplasia resulting from hydroxylase deficiency. J Urol,pp. J Clin Endocrinol Metab, 86pp. Endocr Rev, 15pp.

J Pediatr Surg, 29pp. J Clin Endocrinol Metab, 58pp. J Steroid Biochem Mol Biol, 40pp.

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