Nalini A, Lokesh L, Ratnavalli E
Department of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560 029, India.
J Neurol Sci. 2004 May 15;220(1-2):95-8. doi: 10.1016/j.jns.2004.02.015.
Monomelic amyotrophy (MMA) is a benign lower motor neuron disorder in the young with male preponderance. It is characterized by insidious onset and progressive weakness and wasting of a distal extremity over a few years followed by spontaneous arrest. The exact pathogenesis is unknown. It is predominantly a sporadic disorder but rarely familial forms have been documented. In this report, we describe the phenotype of a 21-year-old man and his mother who were diagnosed to have MMA. The index case presented with left upper limb weakness and wasting of 3 years duration while his mother had right upper limb amyotrophy and weakness of 34 years. A total of 190 patients were diagnosed to have MMA in our institute over the last 27 years and this is the first case of familial MMA.
单肢肌萎缩症(MMA)是一种好发于年轻人的良性下运动神经元疾病,男性更为多见。其特点为隐匿起病,数年中逐渐出现远端肢体无力和萎缩,随后病情自发停止进展。确切的发病机制尚不清楚。该病主要为散发性疾病,但也有罕见的家族性病例报道。在本报告中,我们描述了一名21岁男性及其母亲被诊断为MMA的临床表现。索引病例有3年的左上肢无力和萎缩症状,而他的母亲有34年的右上肢肌萎缩和无力症状。在过去27年里,我院共诊断出190例MMA患者,这是首例家族性MMA病例。