Matsubara S, Yoshino M, Takamori M
Department of Neurology, Kanazawa University School of Medicine, Japan.
J Neurol Neurosurg Psychiatry. 1994 May;57(5):640-2. doi: 10.1136/jnnp.57.5.640.
Two cases of benign neurogenic amyotrophy associated with Klinefelter's syndrome are reported. Both presented with slowly progressive, diffuse neurogenic muscle atrophy of juvenile onset. Both had a karyotype of XXY. Amplification, by the polymerase chain reaction, of a fragment of androgen receptor that was related to bulbospinal muscular atrophy, showed no abnormality. Treatment with androgen in one case provided no benefit. Benign neurogenic amyotrophy in the Klinefelter's syndrome is likely to be an independent type of motor neuron disease and suggests that the X chromosome plays an important part in the biology of motor neurons.
报告了两例与克兰费尔特综合征相关的良性神经源性肌萎缩病例。两例均表现为青少年起病的缓慢进行性、弥漫性神经源性肌肉萎缩。两者的核型均为XXY。通过聚合酶链反应对与延髓脊髓性肌萎缩相关的雄激素受体片段进行扩增,未发现异常。其中一例用雄激素治疗无效。克兰费尔特综合征中的良性神经源性肌萎缩可能是一种独立类型的运动神经元疾病,提示X染色体在运动神经元生物学中起重要作用。