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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| Format: | Article |
| Language: | English |
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Babol University of Medical Sciences
2000-01-01
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| Series: | Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul |
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| Online Access: | http://jbums.org/article-1-2934-en.html |