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








Intervalo de año
1.
Singapore medical journal ; : e92-4, 2012.
Artículo en Inglés | WPRIM | ID: wpr-334477

RESUMEN

Allgrove syndrome is a rare autosomal recessive disorder. It is also known as the 3A syndrome and characterised by the triad of achalasia, alacrima and adrenal insufficiency. The AAAS gene is encoded on chromosome 12q13. We report the case of a 23-year-old woman who presented at the hospital with adrenal crisis that was triggered by infection of the urinary system and gastrointestinal bleeding. She had a known diagnosis of achalasia for eight years, and ophthalmologic examination revealed alacrima. Based on our findings, the patient was diagnosed with Allgrove syndrome.


Asunto(s)
Femenino , Humanos , Adulto Joven , Insuficiencia Suprarrenal , Sangre , Diagnóstico , Genética , Hormona Adrenocorticotrópica , Sangre , Diagnóstico Diferencial , Técnicas de Diagnóstico Oftalmológico , Endoscopía Gastrointestinal , Acalasia del Esófago , Sangre , Diagnóstico , Genética , Mutación , Proteínas del Tejido Nervioso , Sangre , Genética , Proteínas de Complejo Poro Nuclear , Sangre , Genética
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA