Thirty unselected females with proven osteomalacia were evaluated clinically, electromyographically and histopathologically for muscle dysfunction. Clinical evidence of myopathy was found in all the patients except one; the electromyograms were abnormal in 25 of them, and histopathological abnormalities, although slight and nonspecific, were seen in all the 17 patients who underwent muscle biopsy. Electromyographic findings revealed a myopathic pattern as evidenced by a significant reduction in motor unit potential duration and amplitude, and an increased percentage polyphasicity as compared to the controls. There was a complete absence of denervation potentials. The histopathological abnormalities were nonspecific and slight, and consisted of fatty infiltration, interstitial fibrosis, sarcolemmal nuclear proliferation and variation in muscle fibre thickness. A statistically significant reduction in motor nerve conduction velocities of t h e ulnar and pcroneal nerves was found. I t was considered that this reduction in t h e velocities was due to subclinical neuropathy. Our data suggest that myopathy, neuropathy and osteomalacia in our patients are due to nutritional deficiencies of multiple vitamins.