Staal A, Mechelse K
Hum Genet. 1978 May 16;42(1):115-8. doi: 10.1007/BF00291634.
Two brothers with a new type of hereditary sensory neuropathy are described. The main clinical feature is late onset sensory ataxia without ulcerating acropathy or other autonomic abnormality. The older patient also has oculomotor dysfunction and extensor plantar responses.
本文描述了两兄弟患有一种新型遗传性感觉神经病。主要临床特征为迟发性感觉性共济失调,无肢端溃疡或其他自主神经异常。年长患者还存在动眼神经功能障碍和跖伸反射。