| Patient with obstructive sleep apnea-hypopnea syndrome and SCN5A mutation (R1193Q polymorphism) associated with Brugada type 2 electrocardiographic pattern. | |
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MedLine Citation:
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PMID: 18976777 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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We describe a 45-year-old Asian man with Brugada-type 2 electrocardiogram and probable nocturnal agonal respiration. After genetic screening, drug challenge test and polysomnography examination, we ruled out Brugada syndrome and identified obstructive sleep apnea-hypopnea syndrome. Therefore, obstructive sleep apnea-hypopnea syndrome should be considered as a rare differential diagnosis for Brugada syndrome. |
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Authors:
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Xiaoliang Qiu; Wenling Liu; Dayi Hu; Yihong Sun; Lei Li; Cuilan Li |
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Publication Detail:
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Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't Date: 2008-10-30 |
Journal Detail:
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Title: Journal of electrocardiology Volume: 42 ISSN: 1532-8430 ISO Abbreviation: J Electrocardiol Publication Date: 2009 May-Jun |
Date Detail:
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Created Date: 2009-04-28 Completed Date: 2009-07-09 Revised Date: 2009-11-11 |
Medline Journal Info:
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Nlm Unique ID: 0153605 Medline TA: J Electrocardiol Country: United States |
Other Details:
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Languages: eng Pagination: 250-3 Citation Subset: IM |
Affiliation:
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Heart Center, Peking University People's Hospital, Beijing, PR China. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Brugada Syndrome
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complications,
diagnosis*,
genetics* Diagnosis, Differential Electrocardiography / methods* Genetic Predisposition to Disease / genetics Humans Male Middle Aged Mutation / genetics Polymorphism, Single Nucleotide / genetics* Sleep Apnea, Obstructive / complications, diagnosis*, genetics* |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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