Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Más filtros

Banco de datos
Tipo del documento
País de afiliación
Intervalo de año de publicación
1.
N Engl J Med ; 369(2): 164-71, 2013 Jul 11.
Artículo en Inglés | MEDLINE | ID: mdl-23841731

RESUMEN

Although androgen resistance has been characterized in men with a normal chromosome complement and mutations in the androgen-receptor gene, a mutation in the gene encoding estrogen receptor α (ESR1) was previously described only in one man and not, to our knowledge, in a woman. We now describe an 18-year-old woman without breast development and with markedly elevated serum levels of estrogens and bilateral multicystic ovaries. She was found to have a homozygous loss-of-function ESR1 mutation in a completely conserved residue that interferes with estrogen signaling. Her clinical presentation was similar to that in the mouse orthologue knockout. This case shows that disruption of ESR1 causes profound estrogen resistance in women. (Funded by the National Institutes of Health.).


Asunto(s)
Estradiol/sangre , Receptor alfa de Estrógeno/genética , Estrógenos/metabolismo , Mutación Missense , Pubertad Tardía/genética , Adolescente , Glucemia/análisis , Estradiol/administración & dosificación , Receptor alfa de Estrógeno/metabolismo , Estrona/sangre , Femenino , Humanos , Análisis de Secuencia de ADN
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA