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[A case of hereditary sensory and autonomic neuropathy type 1E with frontal lobe dysfunction as an initial symptom].

Rinsho shinkeigaku = Clinical neurology - 27 Dec 2017

Watanabe Masashi, Matsumoto Yushi, Okamoto Kensho, Okuda Bungo, Mizuta Ikuko, Mizuno Toshiki

Abstract excerpt

A 49-year-old man had developed gradually personality change, gait disturbance, and hearing loss for five years. On admission, he presented with frontal release signs, stuttering, vertical gaze palsy, sensorineural deafness, muscle rigidity, ataxia, and sensory disturbance with areflexia in the lower extremities. Brain MRI demonstrated atrophy in the cerebellum and midbrain tegmentum as well as cerebral atrophy,...

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PMID: 29187684
DOI: 10.5692/clinicalneurol.cn-001043

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