Wm. Fowler et al., PROFILES OF NEUROMUSCULAR DISEASES - DESIGN OF THE PROTOCOL, American journal of physical medicine & rehabilitation, 74(5), 1995, pp. 62-69
The purpose of this 10-yr investigation was to develop comprehensive i
mpairment and disability profiles of the clinical characteristics of s
even neuromuscular diseases: spinal muscular atrophy, hereditary motor
sensory neuropathy, Duchenne muscular dystrophy, Becker's muscular dy
strophy, facioscapulohumeral muscular dystrophy, limb-girdle syndrome,
and myotonic dystrophy. Based on the World Health Organization's clas
sification of disablement, as applied to neuromuscular diseases, impai
rment was evaluated by measurements of strength, range of motion, spin
e deformity, cardiac and pulmonary function, and intellectual capacity
. Disability was evaluated by measures of mobility and upper extremity
function, cardiopulmonary adaptations, cardiac and pulmonary complica
tions, and psychosocial adjustment.