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Article: Prevalence and Characteristics of Chinese Patients With Duchenne and Becker Muscular Dystrophy-A Territory Wide Collaborative Study in Hong Kong

TitlePrevalence and Characteristics of Chinese Patients With Duchenne and Becker Muscular Dystrophy-A Territory Wide Collaborative Study in Hong Kong
Authors
Issue Date2015
PublisherSage Publications, Inc..
Citation
Child Neurology Open, 2015, v. 2 n. 2 How to Cite?
AbstractThe aim of this collaborative study on Duchenne muscular dystrophy and Becker muscular dystrophy is to determine the prevalence and to develop data on such patients as a prelude to the development of registry in Hong Kong. Information on clinical and molecular findings, and patient care, was systematically collected in 2011 and 2012 from all Pediatric Neurology Units in Hong Kong. Ninety patients with dystrophinopathy were identified, and 83% has Duchenne muscular dystrophy. The overall prevalence of dystrophinopathy in Hong Kong in 2010 is 1.03 per 10 000 males aged 0 to 24 years. Among the Duchenne group, we observed a higher percentage (40.6%) of point mutations with a lower percentage (45.3%) of exon deletions in our patients when compared with overseas studies. Although we observed similar percentage of Duchenne group received scoliosis surgery, ventilation support, and cardiac treatment when compared with other countries, the percentage (25%) of steroid use is lower.
Persistent Identifierhttp://hdl.handle.net/10722/197618
ISSN

 

DC FieldValueLanguage
dc.contributor.authorChan, SHS-
dc.contributor.authorLo, IFM-
dc.contributor.authorCherek, S-
dc.contributor.authorCheng, WW-
dc.contributor.authorFung, EL-
dc.contributor.authorYeung, WL-
dc.contributor.authorNgan, M-
dc.contributor.authorLee, WC-
dc.contributor.authorKwong, L-
dc.contributor.authorWong, SN-
dc.contributor.authorMa, CK-
dc.contributor.authorTai, SM-
dc.contributor.authorNg, SF-
dc.contributor.authorWu, SP-
dc.contributor.authorWong, VCN-
dc.date.accessioned2014-05-29T08:31:44Z-
dc.date.available2014-05-29T08:31:44Z-
dc.date.issued2015-
dc.identifier.citationChild Neurology Open, 2015, v. 2 n. 2-
dc.identifier.issn2329-048X-
dc.identifier.urihttp://hdl.handle.net/10722/197618-
dc.description.abstractThe aim of this collaborative study on Duchenne muscular dystrophy and Becker muscular dystrophy is to determine the prevalence and to develop data on such patients as a prelude to the development of registry in Hong Kong. Information on clinical and molecular findings, and patient care, was systematically collected in 2011 and 2012 from all Pediatric Neurology Units in Hong Kong. Ninety patients with dystrophinopathy were identified, and 83% has Duchenne muscular dystrophy. The overall prevalence of dystrophinopathy in Hong Kong in 2010 is 1.03 per 10 000 males aged 0 to 24 years. Among the Duchenne group, we observed a higher percentage (40.6%) of point mutations with a lower percentage (45.3%) of exon deletions in our patients when compared with overseas studies. Although we observed similar percentage of Duchenne group received scoliosis surgery, ventilation support, and cardiac treatment when compared with other countries, the percentage (25%) of steroid use is lower.-
dc.languageeng-
dc.publisherSage Publications, Inc..-
dc.relation.ispartofChild Neurology Open-
dc.rightsChild Neurology Open. Copyright © Sage Publications, Inc..-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titlePrevalence and Characteristics of Chinese Patients With Duchenne and Becker Muscular Dystrophy-A Territory Wide Collaborative Study in Hong Kong-
dc.typeArticle-
dc.identifier.emailChan, SHS: sophehs@hku.hk-
dc.identifier.emailKwong, L: kwongl@hkucc.hku.hk-
dc.identifier.emailWong, SN: snwong@hkucc.hku.hk-
dc.identifier.emailWong, VCN: vcnwong@hku.hk-
dc.identifier.authorityWong, VCN=rp00334-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1177/2329048X15585345-
dc.identifier.hkuros229008-
dc.identifier.hkuros232393-
dc.identifier.volume2-
dc.identifier.issue2-
dc.publisher.placeUnited States-
dc.identifier.issnl2329-048X-

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