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Peroneal muscular atrophy with pyramidal tract features (hereditary motor and sensory neuropathy type V): a clinical, neurophysiological, and pathological study of a large kindred.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Yang, Fa-Duan |
| Copyright Year | 1994 |
| Abstract | A large family with autosomal dominant inheritance of peroneal muscular atrophy, associated with extensor plantar responses in some cases, has been studied. Onset was usually in the first two decades and spasticity was not a feature. Nerve conduction studies in 21 cases and light and electron microscope findings on six sural nerve biopsies were similar to those in hereditary motor and sensory neuropathy type II. |
| File Format | PDF HTM / HTML |
| Alternate Webpage(s) | http://jnnp.bmj.com/content/jnnp/57/11/1343.full.pdf |
| PubMed reference number | 7964809v1 |
| Volume Number | 57 |
| Issue Number | 11 |
| Journal | Journal of neurology, neurosurgery, and psychiatry |
| Language | English |
| Access Restriction | Open |
| Subject Keyword | Abducens Nerve Diseases Atrophic Autosomal dominant inheritance Biopsy Charcot-Marie-Tooth Disease Fibromatosis, Plantar Friedreich Ataxia HMN (Hereditary Motor Neuropathy) Proximal Type I Hereditary Motor and Sensory Neuropathies Microscopes Muscle Spasticity Muscular Atrophy Optic Nerve Glioma, Childhood Plantar - anatomical location Pyramidal Tracts Sensory neuropathy Structure of sural nerve electron microscope nervous system disorder |
| Content Type | Text |
| Resource Type | Article |