Long QT syndrome in chromosome 7q35q36.3 deletion involving KCNH2 gene: Warning for chlorpheniramine prescription

Long QT syndrome in chromosome 7q35q36.3 deletion involving KCNH2 gene: Warning for chlorpheniramine prescription

Abstract Background The deletion of the distal 7q region is a rare chromosomal syndrome characterized by wide phenotypic manifestations including growth and psychomotor delay, facial dysmorphisms, and genitourinary malformations. Methods We describe a 6‐year‐old child with a 12‐Mb deletion of the re...

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Bibliographic Details
Main Authors: Giuseppe Di Stolfo, Maria Accadia, Sandra Mastroianno, Maria P. Leone, Orazio Palumbo, Pietro Palumbo, Domenico Potenza, Pasquale Maccarone, Michele Sacco, Aldo Russo, Massimo Carella
Format: Article
Language:English
Published: Wiley 2019-09-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
chlorpheniramine
chromosome 7q35q36.3 deletion
long QT syndrome
syncope
Online Access:https://doi.org/10.1002/mgg3.855

Internet

https://doi.org/10.1002/mgg3.855

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