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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| Formato: | article |
| Lenguaje: | EN FA |
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Babol University of Medical Sciences
2000
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| Acceso en línea: | https://doaj.org/article/72d3bd83889b4223ad99ef059ac866b8 |
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