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

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 long QT int...

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Detalles Bibliográficos
Autores principales:	Adadi, N., Lahrouchi, N., Bouhouch, R., Fellat, I., Amri, R., Alders, M., Sefiani, A., Bezzina, C., Ratbi, I.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2017
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376485/ https://www.ncbi.nlm.nih.gov/pubmed/28364778 http://dx.doi.org/10.1186/s13256-017-1243-1

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