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Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: Confirmation of a new entity

โœ Scribed by Sabatelli, M.; Mignogna, T.; Lippi, G.; Servidei, S.; Zollino, M.; Padua, L.; Monaco, M. Lo; De Armas, L.; Mereu, M.L.; Tonali, P.


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
25 KB
Volume
75
Category
Article
ISSN
0148-7299

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โœฆ Synopsis


We describe two brothers, 11 and 13 years old, respectively, with an early-onset hereditary motor and sensory neuropathy, deafness, and mental retardation. Electrophysiological studies showed marked reduction of motor and sensory conduction velocity and absence of sensory action potentials. Sural nerve biopsy, performed in both patients, showed absence of large myelinated fibers with normal density of small myelinated fibers without axonal degeneration. Signs of demyelination were found only in the younger patient. We suggest that motorsensory neuropathy associated with deafness and mental retardation with absence of large myelinated fibers on sural nerve biopsy represents a distinct clinicopathological entity, which is transmitted in families probably as an autosomal recessive trait. Am.


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X-linked motor-sensory neuropathy type-I
โœ Cowchock, F. Susan ;Duckett, Serge W. ;Streletz, Leopold J. ;Graziani, Leonard J ๐Ÿ“‚ Article ๐Ÿ“… 1985 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 562 KB

We report on a family with an apparently X-linked neuromuscular disease. Electrophysiologic tests and electron microscopic studies are consistent with the diagnosis of hereditary motor sensory neuropathy type 11 , one form of Charcot-Marie-Tooth disease. The manner of inheritance, the observation th