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Int J Pediatr Otorhinolaryngol ; 39(2): 163-8, 1997 Mar 06.
Article in English | MEDLINE | ID: mdl-9104625

ABSTRACT

A family with two of its members having Jervell and Lange-Nielsen syndrome is reported for the first time from Saudi Arabia. A history of syncopal attack in a child with hearing loss and the sudden death of her brother while playing suggested the possibility of the syndrome. Electrocardiogram and full ENT and audiological assessment revealed Jervell and Lange-Nielsen syndrome in the living child. Treatment was given and the condition is now under control.


Subject(s)
Long QT Syndrome/diagnosis , Long QT Syndrome/genetics , Adrenergic beta-Antagonists/therapeutic use , Child, Preschool , Electrocardiography , Female , Hearing Loss, Sensorineural/diagnosis , Heart/physiopathology , Humans , Pedigree , Saudi Arabia , Syncope/diagnosis , Syncope/drug therapy , Syncope/physiopathology
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