A boy with Prader-Willi syndrome: unmasking precocious puberty during growth hormone replacement therapy
Arch. endocrinol. metab. (Online); 60 (6), 2016
SUMMARY Prader-Willi syndrome (PWS) is a genetic disorder frequently characterized by obesity, growth hormone deficiency, genital abnormalities, and hypogonadotropic hypogonadism. Incomplete or delayed pubertal development as well as premature adrenarche are usually found in PWS, whereas central precocio...
Metilación de ADN, Hormona Liberadora de Gonadotropina/uso terapéutico, Terapia de Reemplazo de Hormonas/métodos, Hormona de Crecimiento Humana/uso terapéutico, Síndrome de Prader-Willi/diagnóstico, Síndrome de Prader-Willi/tratamiento farmacológico, Síndrome de Prader-Willi/genética, Pubertad Precoz/complicaciones, Pubertad Precoz/tratamiento farmacológico, Proteínas Recombinantes/efectos adversos, Proteínas Recombinantes/uso terapéutico