Muthukrishnan J, Harikumar K V S, Sangeeta J, Singh M K, Modi K
Department of Endocrinology, Medwin Hospital, Chirag Ali Lane, Nampally, Hyderabad 500001, India.
Singapore Med J. 2009 Aug;50(8):e293-4.
Severe muscle weakness in osteomalacia may mimic a primary neuromuscular disorder like spinal muscular atrophy. A 32-year-old woman, initially diagnosed as a case of spinal muscular atrophy based on clinical presentation, electromyography and muscle biopsy, was later found to have osteomalacic myopathy due to primary hyperparathyroidism complicated by vitamin D deficiency. Before diagnosing a progressive, inevitably fatal degenerative condition like spinal muscular atrophy, one must rule out all possible treatable conditions with a similar presentation.
骨软化症中的严重肌肉无力可能会酷似原发性神经肌肉疾病,如脊髓性肌萎缩症。一名32岁女性,最初根据临床表现、肌电图和肌肉活检被诊断为脊髓性肌萎缩症,后来发现是由于原发性甲状旁腺功能亢进并发维生素D缺乏所致的骨软化性肌病。在诊断像脊髓性肌萎缩症这样进展性、不可避免会致命的退行性疾病之前,必须排除所有具有相似表现的可能可治疗的疾病。