Hereditary Motor Sensory Neuropathies in Childhood
- 12 November 2008
- journal article
- research article
- Published by Wiley in Developmental Medicine and Child Neurology
- Vol. 25 (1) , 19-31
- https://doi.org/10.1111/j.1469-8749.1983.tb13718.x
Abstract
Clinical data on 24 patients with hereditary motor sensory neuropathies, with onset in the pediatric period, and of their relatives is reported. Electrophysiological studies were done in all patients and in 15 relatives. The patients were divided into 2 groups (types I and II) and their hereditary trait was determined. In 11 patients a sural nerve biopsy was performed and revealed different patterns of histological alterations. The nerve biopsy always confirmed the value of conduction velocity in distinguishing between types I and II. A genetic discordance was observed, both in regard to the phenotype and the conduction velocity, and there was increased slowing of the conduction velocity as individuals grew older. The classification of these disorders in childhood can be particularly difficult. The role of sural nerve biopsy is discussed.This publication has 18 references indexed in Scilit:
- POOLED EUROPEAN SERIES OF HEREDITARY PERIPHERAL NEUROPATHIES IN INFANCY AND CHILDHOODNeuropediatrics, 1981
- Autosomal recessive forms of hereditary motor and sensory neuropathy.Journal of Neurology, Neurosurgery & Psychiatry, 1980
- THE CLINICAL FEATURES OF HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPES I AND IIBrain, 1980
- Hereditary Motor and Sensory Neuropathy Type I in Infancy and Childhood: A Clinical, Electrodiagnostic, Genetic and Muscle Biopsy StudyNeuropediatrics, 1979
- CLINICAL AND ELECTRODIAGNOSTIC FEATURES OF CHARCOT-MARIE-TOOTH SYNDROMEActa Neurologica Scandinavica, 1978
- PERONEAL MUSCULAR ATROPHY (PMA) AND RELATED DISORDERSBrain, 1977
- PERONEAL MUSCULAR ATROPHY (PMA) AND RELATED DISORDERSBrain, 1977
- Hereditary motor and sensory polyneuropathy (peroneal muscular atrophy)*Annals of Human Genetics, 1974
- Motor nerve conduction velocity in peroneal muscular atrophy: evidence for genetic heterogeneityJournal of Neurology, Neurosurgery & Psychiatry, 1974
- NERVE CONDUCTION STUDIES IN CHARCOT-MARIE-TOOTH DISEASEActa Neurologica Scandinavica, 1972