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












Base de datos
Intervalo de año de publicación
1.
Zhonghua Yi Xue Za Zhi ; 104(16): 1347-1350, 2024 Apr 23.
Artículo en Chino | MEDLINE | ID: mdl-38644281

RESUMEN

Alport syndrome is one of the most common inherited kidney diseases caused by mutations in the type Ⅳ collagen genes. It has a complex pattern of inheritance and diverse clinical manifestations, and severe cases will rapidly progress to end-stage kidney disease. With the rapid development of genetic testing technology, there is a deeper understanding of the genetic spectrum of Alport syndrome, the effectiveness of clinical therapies, and the prediction of disease prognosis. Therefore, the purpose of the article is to introduce the advances in the diagnosis and treatment of Alport syndrome, aiming to improve the early diagnosis and standardized treatment of this disease.


Asunto(s)
Colágeno Tipo IV , Mutación , Nefritis Hereditaria , Nefritis Hereditaria/terapia , Nefritis Hereditaria/diagnóstico , Nefritis Hereditaria/genética , Humanos , Colágeno Tipo IV/genética , Pruebas Genéticas , Pronóstico , Fallo Renal Crónico/terapia , Fallo Renal Crónico/genética , Fallo Renal Crónico/diagnóstico
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...