Prevalence and Characteristics of Chinese Patients With Duchenne and Becker Muscular Dystrophy

Author:

Chan Sophelia H. S.1,Lo Ivan F. M.2,Cherk Sharon W. W.3,Cheng Wai Wai4,Fung Eva L. W.5,Yeung Wai Lan6,Ngan Mary7,Lee Wing Cheong7,Kwong Ling7,Wong Suet Na8,Ma Che Kwan8,Tai Shuk Mui9,Ng Grace S. F.10,Wu Shun Ping11,Wong Virginia C. N.1

Affiliation:

1. Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong SAR, China

2. Department of Health, Clinical Genetic Services, Hong Kong SAR, China

3. Department of Paediatrics and Adolescent Medicine, Kwong Wah Hospital, Hong Kong SAR, China

4. Department of Paediatrics and Adolescent Medicine, Caritas Medical Centre, Hong Kong SAR, China

5. Department of Paediatrics, Prince of Wales Hospital, Chinese University of Hong Kong, Hong Kong SAR, China

6. Department of Paediatrics and Adolescent Medicine, Alice Ho Miu Ling Nethersole Hospital, Hong Kong SAR, China

7. Department of Paediatrics and Adolescent Medicine, Tuen Mun Hospital, Hong Kong SAR, China

8. Department of Paediatrics and Adolescent Medicine, United Christian Hospital, Hong Kong SAR, China

9. Department of Paediatrics and Adolescent Medicine, Pamela Youde Nethesole Eastern Hospital, Hong Kong SAR, China

10. Department of Paediatrics and Adolescent Medicine, Princess Margaret Hospital, Hong Kong SAR, China

11. Department of Paediatrics and Adolescent Medicine, Queen Elizabeth Hospital, Hong Kong SAR, China

Abstract

The 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.

Publisher

SAGE Publications

Subject

General Economics, Econometrics and Finance

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