Alberca R, Chinchón I, Rafel E, Gil-Neciga E
Servicio de Neurología y Dto, de Anatomía Patológica, HU Virgen del Rocío, Sevilla.
Arch Neurobiol (Madr). 1990 Mar-Apr;53(2):92-5.
A 31-year-old female had since childhood walking difficulties on her right foot. She subsequently developed a right-sided scapuloperoneal amyotrophy with mild distal sensory sings. Nerve conduction velocities and nerve biopsy showed a peripheral neuropathy, and the case was thought to be an example of Davidenkow's syndrome. At the age of 41, the musculature innervated by the right V, VII, XI and XIIth cranial nerves became impaired and this suggested that the lower motor neuron was also involved precluding this picture from inclusion among the Hereditary Motor and Sensory Neuropathies (HMSN) to which Davidenkow's syndrome has been related.
一名31岁女性自幼右脚行走困难。随后她出现了右侧肩胛腓骨肌萎缩，并伴有轻度远端感觉症状。神经传导速度和神经活检显示为周围神经病变，该病例被认为是戴维登科夫综合征的一个例子。41岁时，右侧第V、VII、XI和XII对脑神经支配的肌肉组织出现功能障碍，这表明下运动神经元也受到了影响，从而排除了将此病例归为与戴维登科夫综合征相关的遗传性运动和感觉神经病变（HMSN）的可能性。
