Author/Authors :
Gritli، نويسنده , , Sami and Ben Salah، نويسنده , , Mamia and Shili، نويسنده , , Abdessalem and Robson، نويسنده , , Caroline D. and Ferjaoui، نويسنده , , Mohamed and Hendaoui، نويسنده , , Lotfi and Belhani، نويسنده , , Ali and Jilani، نويسنده , , Sarrah Baltagi-Ben and Gusella، نويسنده , , James F. and MacRae، نويسنده , , Calum A.، نويسنده ,
Abstract :
We report on the long QT syndrome occurring in conjunction with nontoxic multinodular goiter and sensorineural deafness in several siblings of a large family. Autosomal and X-linked recessive and dominant modes of inheritance are possible for the different phenotypes. The affected family members had various phenotype combinations, suggesting variable expressivity and incomplete penetrance.
