Literature DB >> 1331333

Detection of hereditary motor sensory neuropathy type I in childhood.

T E Feasby1, A F Hahn, C F Bolton, W F Brown, W J Koopman.   

Abstract

Clinical signs and slowed motor nerve conduction velocities were found in 17 of 36 children under 10 years of age who had one parent with hereditary motor sensory neuropathy type I (HMSN I). Four children had slowed conduction velocities at one year or less. Clinical signs were subtle and included pes planus, distal foot wasting, weakness of ankle eversion and dorsiflexion and areflexia. HMSN I can be detected reliably in children, even before one year of age.

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Year:  1992        PMID： 1331333      PMCID： PMC1015184          DOI： 10.1136/jnnp.55.10.895

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


  14 in total

1.  NORMAL CONDUCTION VELOCITY OF ULNAR, MEDIAN AND PERONEAL NERVES IN INFANCY, CHILDHOOD AND ADOLESCENCE.

Authors:  I GAMSTORP
Journal:  Acta Paediatr Suppl       Date:  1963

2.  Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.

Authors:  P J Dyck; E H Lambert
Journal:  Arch Neurol       Date:  1968-06

3.  Motor nerve conduction velocity in peroneal muscular atrophy: evidence for genetic heterogeneity.

Authors:  P K Thomas; D B Calne
Journal:  J Neurol Neurosurg Psychiatry       Date:  1974-01       Impact factor: 10.154

4.  Localization of a locus for Charcot-Marie-Tooth neuropathy type Ia (CMT1A) to chromosome 17.

Authors:  P J McAlpine; T E Feasby; A F Hahn; L Komarnicki; S James; C Guy; M Dixon; S Qayyum; J Wright; G Coopland
Journal:  Genomics       Date:  1990-07       Impact factor: 5.736

5.  Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations.

Authors:  P J Dyck; E H Lambert
Journal:  Arch Neurol       Date:  1968-06

6.  The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood.

Authors:  R A Ouvrier; J G McLeod; T E Conchin
Journal:  Brain       Date:  1987-02       Impact factor: 13.501

7.  Linkage evidence for genetic heterogeneity among kinships with hereditary motor and sensory neuropathy, type I.

Authors:  P J Dyck; J Ott; S B Moore; C J Swanson; E H Lambert
Journal:  Mayo Clin Proc       Date:  1983-07       Impact factor: 7.616

8.  The application of nerve conduction and clinical studies to genetic counseling in hereditary motor and sensory neuropathy type I.

Authors:  J Berciano; O Combarros; J Calleja; J M Polo; C Leno
Journal:  Muscle Nerve       Date:  1989-04       Impact factor: 3.217

9.  Dominantly inherited peroneal muscular atrophy (hereditary motor and sensory neuropathy type I) in infancy and childhood.

Authors:  M Vanasse; V Dubowitz
Journal:  Muscle Nerve       Date:  1981 Jan-Feb       Impact factor: 3.217

10.  Longitudinal study of neuropathic deficits and nerve conduction abnormalities in hereditary motor and sensory neuropathy type 1.

Authors:  P J Dyck; J L Karnes; E H Lambert
Journal:  Neurology       Date:  1989-10       Impact factor: 9.910
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  1 in total

Review 1.  Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease.

Authors:  D Pareyson; V Scaioli; M Laurà
Journal:  Neuromolecular Med       Date:  2006       Impact factor: 3.843
  1 in total

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