Callaú BA

Idioma: Español
Referencias bibliográficas: 12
Paginas: 371-374
Archivo PDF: 167.17 Kb.

RESUMEN

The late onset congenital adrenal hyperplasia, also called Nonclassic, has a much milder clinical presentation than the classic “Salt wasting form”, and is a condition that may go unnoticed or mistaken for polycystic ovary syndrome. The history of newborn screening is not reliable to rule out its presence and if suspected, measurements must be performed (17-hydroxyprogesterone). The treatment of this disease has proven to be useful because it improves the fertility of the affected people but are not yet duly filed regimes.

REFERENCIAS (EN ESTE ARTÍCULO)

1. Azziz R, Dewailly D, Owerbach D. Nonclassic adrenal hyperplasia: current concepts. Clinical review 374 REVISTA MEDICA DE COSTA RICA Y CENTROAMERICA 56. J Clin Endocrinol Metab 1996;78:810-815.

2. Escobar-Morreale H, Sanchon R, San Millán J. A prospective study of the prevalence of nonclassical congenital adrenal hyperplasia among women presenting with hyperandrogenic symptoms and signs. J Clin Endocrinol Metab 2008; 93: 527-33.

3. Gardner, D & Shoback, D. (2012) Hipertensión endocrina. En D. Cooper, Endocrinología Básica y Clínica de Greenspan (9° Ed p 340). Mexico DF.

4. Kliegman R, Behrman R, Jenson H & Stanton B. (2008) Hiperplasia suprarrenal congénita y trastornos relacionados. Nelson Tratado de Pediatría (18° Ed pp 2360-2366). Madrid.

5. Melmed S, Polonsky K, Larsen P. & Kronenberg H. (2011). The Adrenal cortex. En G. Brent & T. Davies, Williams Textbook of Endocrinology (12° Ed pp 525-526) Philadelphia.

6. New M. Infertility and androgen excess in nonclassical 21-hydroxylase deficiency. Symposium on the ovary: regulation, dysfunction and treatment, Marco Island, FL. 1996: 195-8. 6.

7. Pombo M & Arjemí J (1997) Anomalías de la diferenciación sexual. En Audí L, Tratado de endocrinología Pediátrica. (2° Ed p 826) Madrid.

8. Sanchez A, Salvador E & Ramirez A. (2010) Hiperplasia suprarrenal congénita de inicio tardío y síndrome de ovarios poliquísticos. Igual fenotipo diferente origen y destino. Instituto Nacional de Perinatología Isidro Espinosa de los Reyes. Volumen 24, Número 4 pp 221-227.

9. Speiser P, Knochenhauer E, Dewailly D, Fruzzetti F, Marcondes J, Azziz R. A multicenter study of women with nonclassical congenital hyperplasia: relationship between genotype and phenotype. Mol Gen Metabol 2000; 71: 527-34.

10. Speiser PW, White PC. Congenital adrenal hyperplasia. N Engl J Med 2008; 349: 776-88.

11. White PC, Speiser PW. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Endocr Rev 2000;21:245-291.

12. Zerah M, Ueshiba H, Wood E,Speiser PW, Crawford C, McDonald T, Pareira J, Gruen D, new MI. Prevalence of nonclassical steroid 21-hydroxylase deficiency based on a morning salivary 17-hydroxyprogesterone screening test: a small sample study. J Clin Endocrinol Metab 1990; 70: 1662-7.