J Korean Acad Rehabil Med.
2001 Apr;25(2):241-248.
Clinical Profile of Duchenne Muscular Dystrophy
- Affiliations
-
- 1Department of Rehabilitation Medicine and Rehabilitation Institute of Muscular disease.
- 2Yonsei University College of Medicine.
- 3Department of Rehabilitation Medicine, Soonchunhyang University College of Medicine.
- 4Department of Rehabilitation Medicine, Inje University College of Medicine.
Abstract
OBJECTIVE
To evaluate clinical features in general and possible complications in Duchenne muscular dystrophy (DMD) which could be used for comprehensive rehabilitation management.
METHOD: One hundred and seventy-two patients with DMD were followed over 3 year period to
provide clinical profile causing impairment and disability. We measured height, weight and manual
muscle testing (MMT) when the patients visited the hospital. And we could measure pulmonary
function, electrocardiogram (EKG), and intelligence quotient (IQ) test in cooporative patients.
RESULTS
The median height and weight of DMD boys were normally distributed before age
12, but during the second decade height was markedly reduced, and weight was no longer
normally distributed. The MMT measurement showed loss of strength in a fairly linear fashion
according to increasing age, and extensor of lower extremities were weaker than flexors showing
typical contractures of legs. There was a direct relationship between pulmonary function and
MMT scores of upper extremities. There was a high occurrence (40%) of abnormal EKG, but
none of the patients had a history of cardiovascular complication. DMD children suffered wide
spectrum of psychological disturbance such as somatic complaints, attention and emotional
problems in addition to expected psychological problems due to chronic disease and its
progression, and 50.9% of them were below average on the IQ test.
CONCLUSION
These data on DMD subjects provide clinicians with useful information regarding
the prevalence and severity of measurable impairment at different stages of the disease.