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

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 region 7q...

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Detalles Bibliográficos
Autores principales: Di Stolfo, Giuseppe, Accadia, Maria, Mastroianno, Sandra, Leone, Maria P., Palumbo, Orazio, Palumbo, Pietro, Potenza, Domenico, Maccarone, Pasquale, Sacco, Michele, Russo, Aldo, Carella, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732270/
https://www.ncbi.nlm.nih.gov/pubmed/31347270
http://dx.doi.org/10.1002/mgg3.855

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732270/
https://www.ncbi.nlm.nih.gov/pubmed/31347270
http://dx.doi.org/10.1002/mgg3.855

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