Aims: Duchenne muscular dystrophy (DMD), an inherited X-linked muscular disease, is associated with dilated cardiomyopathy that is responsible for death in 40% of patients. Our objective was to determine whether inotropic reserve is predictive of LV trend over time.
Methods And Results: A total of 69 DMD patients (age 12.
Introduction: Upper limb evaluation of patients with Duchenne Muscular Dystrophy is crucially important to evaluations of efficacy of new treatments in non-ambulant patients. In patients who have lost ambulation, there are few validated and informative outcome measures. In addition, longitudinal data demonstrating sensitivity to clinical evolution of outcome measures over short-term periods are lacking.
View Article and Find Full Text PDFThe child comes in specialist consultation very often. Only after a good examination, we can quiet parents. Flatfoot, cavus foot toewalking can be alone symptom for a general disease.
View Article and Find Full Text PDFActa Orthop Traumatol Turc
October 2006
A new series of 350 previously unreported cases of clubfoot treated by the functional method are reported. One hundred and eighteen clubfeet were unilateral and 116 were bilateral. The follow-up ranged from 11 to 18 years, with an average of 14 years.
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