A case report of Jervell Neilson syndrome in Babol
Objective: Jervell Neilson syndrome is a rare congenital disease, which manifests with prolonged QT-interval, deafness and recurrent syncope. This disease is transmitted in autosomal recessive form and in this paper we report a rare case of Jervell Neilson syndrome with recurrent syncope and deafnes...
Guardado en:
Autor principal: | |
---|---|
Formato: | article |
Lenguaje: | EN FA |
Publicado: |
Babol University of Medical Sciences
2000
|
Materias: | |
Acceso en línea: | https://doaj.org/article/72d3bd83889b4223ad99ef059ac866b8 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|