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...

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Autor principal: Kh Amou Zadeh
Formato: article
Lenguaje:EN
FA
Publicado: Babol University of Medical Sciences 2000
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R
Acceso en línea:https://doaj.org/article/72d3bd83889b4223ad99ef059ac866b8
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