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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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| Publicado no: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6732270/ https://ncbi.nlm.nih.gov/pubmed/31347270 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.855 |
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