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AAEE case report #20: Hereditary motor and sensory neuropathy, type I

✍ Scribed by David A. Chad


Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
698 KB
Volume
12
Category
Article
ISSN
0148-639X

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Patients affected with hereditary motor sen. sory neuropathy (HMNS) type I were traced through hospital records. Each case was reexamined, a family history was drawn, and EMG examination was performed in those members of the family who could have inherited the trait. In the prevalence year 1987, in

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Facial nerve function was studied in 19 patients with hereditary motor and sensory neuropathy type I (HMSN I) and 2 patients with hereditary motor and sensory neuropathy type III (HMSN III, DΓ©jΓ©rine-Sottas), and compared to that in 24 patients with Guillain-BarrΓ© syndrome (GBS). The facial nerve was

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A 30-year-old male with hereditary motor and sensory neuropathy, type I (HMSN I), presented with asymmetric weakness of finger extension and radial deviation with left wrist extension, previously felt to be a manifestation of the peripheral neuropathy. Nerve conduction studies confirmed HMSN I; howe

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Motor conduction studies were performed serially in 10 patients, ages 10-62 years, with clinical and electrophysiological criteria of hereditary motor and sensory neuropathy type 1 (HMSN-1) over periods of 11-19 years. Median nerve conduction velocity (MNCV) and distal motor latency showed no signif