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.

Author: Shakalabar Gom
Country: Algeria
Language: English (Spanish)
Genre: Politics
Published (Last): 1 December 2008
Pages: 144
PDF File Size: 6.93 Mb
ePub File Size: 6.60 Mb
ISBN: 222-3-84451-131-3
Downloads: 94831
Price: Free* [*Free Regsitration Required]
Uploader: Faum

J Paediatr Child Health, 31pp. Acta Paediatr,pp. Protoc diagn ter pediatr. Pregnancy outcomes in women with congenital virilizing adrenal hyperplasia. J Pediatr Endocrinol Metab, 7pp. Clin Endocrinol, 51pp.

New therapeutic options are currently under investigation, including the use of antiandrogens, estrogen synthesis inhibitors, and adrenalectomy. Sistema OJS – Metabiblioteca. A continuum of disorders. Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to hydroxylase deficiency. Clin Endocrinol Oxf43pp. The interrelationship of sodium balance, plasma renin activity and ACTH in congenital adrenal hyperplasia.

Clin Endocrinol Oxf42pp. Over the long-term course of the disease, these patients can develop a series of complications that include short stature, obesity, reduced congenjta mineral density, gonadal dysfunction, infertility and psychosexual dysfunction in women. Arq Bras Endocrinol Metab. True precocious puberty complicating congenital adrenal hyperplasia: J Clin Endocrinol Metab, 86pp.


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

An asymptomatic male sibling was disclosed after molecular study. Male pseudohermaphroditism due to 5 alpha-reductase-2 deficiency in an Arab kindred. Junho Documento Ant — Documento Seg. Bone turnover and bone mineral density in patients with congenital adrenal hyperplasia.


Adrenal incidentaloma and patients with homozygous or heterozygous congenital adrenal hyperplasia. The present article reviews the diagnostic and therapeutic features of congenital adrenal hyperplasia with special emphasis on hydroxylase deficiency and its long-term outcome. Suprargenal final en pacientes con hiperplasia suparrenal congenita.

J Clin Endocrinol Metab, 82pp. Mineralocorticoids in congenital adrenal hyperplasia. Endocrinologia, 41pp. Prophylactic adrenalectomy of a three-year-old girl with congenital adrenal hyperplasia: Rapid second-tier molecular genetic analysis for congenital adrenal suprarrenal attributable to steroid hydroxylase deficiency.

Height outcome in congenital adrenal hyperplasia caused by 21 hydroxylase deficiency: Close genetic linkage between HLA and congenital adrenal hyperplasia hydroxylase deficiency. J Pediatr Child Health, 29pp.


Alonso M, Ezquieta B.

Recuperado a partir de https: J Ped Endocrinol Metab, 11pp. Hipefplasia laparoscopic adrenalectomy as a treatment for classic congenital adrenal hyperplasia attributable to hydroxylase deficiency abstract. Treatment aims to decrease adrenocorticotropic hormone secretion and underlying adrenal hyperandrogenism and to correct the glucocorticoid and mineralocorticoid deficiency as physiologically as possible.

Prenatal treatment of congenital adrenal hyperplasia resulting from hydroxylase deficiency. J Clin Endocrinol Metab, 78pp. Patients with prepubertal or pubertal diagnosis.

Randomised controlled trial of growth effect of hydrocortisone in hiperplasia suprarrenal congenita adrenal hyperplasia. An update on the molecular genetics of congenital adrenal hyperplasia: Analysis conngenita steroid hydroxylase gene in the Spanish population.