## Abstract A patient with Ewing's sarcoma and demyelinating type CharcotβMarieβTooth disease (CMT) developed severe neuropathy after receiving a total vincristine dose of 6 mg. Recovery was slow and incomplete. A second patient with axonal type CMT developed moderate neuropathy but tolerated exten
Hereditary motor and sensory neuropathy type I and type II
β Scribed by A. Sghirlanzoni; D. Pareyson; V. Scaioli; R. Marazzi; L. Pacini
- Publisher
- Springer Milan
- Year
- 1990
- Tongue
- English
- Weight
- 683 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1590-1874
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
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
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