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

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作者： Giuseppe,Di Stolfo ^[1] ; Maria,Accadia ^[2] ; Sandra,Mastroianno ^[1] ; Maria P,Leone ^[3] ; Orazio,Palumbo ^[3] ; Pietro,Palumbo ^[3] ; Domenico,Potenza ^[1] ; Pasquale,Maccarone ^[4] ; Michele,Sacco ^[4] ; Aldo,Russo ^[1] ; Massimo,Carella ^[3]

作者单位： Cardiovascular Department, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Foggia, Italy. ^[1] Medical Genetics Service, Hospital "Cardinale G. Panico", Tricase, Lecce, Italy. ^[2] Division of Medical Genetics, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Foggia, Italy. ^[3] Paediatric Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Foggia, Italy. ^[4]

关键词 chlorpheniramine chromosome 7q35q36.3 deletion long QT syndrome syncope

主题词儿童(Child);氯苯那敏(Chlorpheniramine);染色体缺失(Chromosome Deletion);染色体, 人, 7对(Chromosomes, Human, Pair 7);DNA拷贝数变异(DNA Copy Number Variations);药物处方(Drug Prescriptions);心电描记术(Electrocardiography);遗传关联研究(Genetic Association Studies);疾病遗传易感性(Genetic Predisposition to Disease);人类(Humans);QT延长综合征(Long QT Syndrome);男(雄)性(Male)

DOI 10.1002/mgg3.855

PMID 31347270

发布时间 2021-01-10

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Molecular genetics & genomic medicine

2019年7卷9期

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

Molecular genetics & genomic medicine

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Molecular genetics & genomic medicine

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

Molecular genetics & genomic medicine

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Molecular genetics & genomic medicine

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