Clinical and molecular findings in a Moroccan family with Jervell and Lange-Nielsen syndrome: a case report

Abstract Background Jervell and Lange-Nielsen syndrome (Online Mendelian Inheritance in Man 220400) is a rare autosomal recessive cardioauditory ion channel disorder that affects 1/200,000 to 1/1,000,000 children. It is characterized by congenital profound bilateral sensorineural hearing loss, a lon...

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Autors principals:	N. Adadi, N. Lahrouchi, R. Bouhouch, I. Fellat, R. Amri, M. Alders, A. Sefiani, C. Bezzina, I. Ratbi
Format:	Artigo
Idioma:	Inglês
Publicat:	BMC 2017-04-01
Col·lecció:	Journal of Medical Case Reports
Matèries:	Jervell and Lange-Nielsen syndrome Long QT syndrome Deafness Moroccan Mutation
Accés en línia:	http://link.springer.com/article/10.1186/s13256-017-1243-1
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