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
Materias:	sensory deafness syncope cardiac syncope prolonged qt-interval Medicine R Medicine (General) R5-920
Acceso en línea:	https://doaj.org/article/72d3bd83889b4223ad99ef059ac866b8
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id	oai:doaj.org-article:72d3bd83889b4223ad99ef059ac866b8
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spelling	oai:doaj.org-article:72d3bd83889b4223ad99ef059ac866b82021-11-10T09:22:00ZA case report of Jervell Neilson syndrome in Babol1561-41072251-7170https://doaj.org/article/72d3bd83889b4223ad99ef059ac866b82000-01-01T00:00:00Zhttp://jbums.org/article-1-2934-en.htmlhttps://doaj.org/toc/1561-4107https://doaj.org/toc/2251-7170Objective: 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 deafness. Case: A 14-year boy, which had neural deafness since childhood referred with recurrent episodes of syncope. On physical examination, blood pressure, jugular venous pulse, the first and the second heart sounds were normal. Chest X-ray and ECHO-Cardiography were also normal. In ECG, there was prolonged QT interval. He was treated with beta-blocker agents and had no syncope after 3 years on follow up. Conclusion: Jervell Neilson syndrome must be considered in differential diagnosis of childhood syncope in order to prevent cardiac syncope complications.Kh Amou ZadehBabol University of Medical Sciencesarticlesensory deafnesssyncopecardiac syncopeprolonged qt-intervalMedicineRMedicine (General)R5-920ENFAMajallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, Vol 2, Iss 1, Pp 53-55 (2000)
institution	DOAJ
collection	DOAJ
language	EN FA
topic	sensory deafness syncope cardiac syncope prolonged qt-interval Medicine R Medicine (General) R5-920
spellingShingle	sensory deafness syncope cardiac syncope prolonged qt-interval Medicine R Medicine (General) R5-920 Kh Amou Zadeh A case report of Jervell Neilson syndrome in Babol
description	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 deafness. Case: A 14-year boy, which had neural deafness since childhood referred with recurrent episodes of syncope. On physical examination, blood pressure, jugular venous pulse, the first and the second heart sounds were normal. Chest X-ray and ECHO-Cardiography were also normal. In ECG, there was prolonged QT interval. He was treated with beta-blocker agents and had no syncope after 3 years on follow up. Conclusion: Jervell Neilson syndrome must be considered in differential diagnosis of childhood syncope in order to prevent cardiac syncope complications.
format	article
author	Kh Amou Zadeh
author_facet	Kh Amou Zadeh
author_sort	Kh Amou Zadeh
title	A case report of Jervell Neilson syndrome in Babol
title_short	A case report of Jervell Neilson syndrome in Babol
title_full	A case report of Jervell Neilson syndrome in Babol
title_fullStr	A case report of Jervell Neilson syndrome in Babol
title_full_unstemmed	A case report of Jervell Neilson syndrome in Babol
title_sort	case report of jervell neilson syndrome in babol
publisher	Babol University of Medical Sciences
publishDate	2000
url	https://doaj.org/article/72d3bd83889b4223ad99ef059ac866b8
work_keys_str_mv	AT khamouzadeh acasereportofjervellneilsonsyndromeinbabol AT khamouzadeh casereportofjervellneilsonsyndromeinbabol
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A case report of Jervell Neilson syndrome in Babol

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