Literature DB >> 191348

A new variety of hereditary sensory neuropathy.

G C Robinson, J E Jan, J R Miller.   

Abstract

A pedigree with a new form of hereditary sensory neuropathy is described. Ataxia and scoliosis rather than loss of pain and ulcerating acropathy are the principal clinical feature. Analysis of the pedigree suggests a dominant mode of transmission with variable age of onset and perhaps reduced penetrance.

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Mesh：

Year:  1977        PMID： 191348     DOI： 10.1007/bf00393964

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  5 in total

1.  Infantile polymyoclonus: Its occurrence in second cousins.

Authors:  G C Robinson; J E Jan; H G Dunn
Journal:  Clin Genet       Date:  1976-01       Impact factor: 4.438

2.  Hereditary sensory radicular neuropathy.

Authors:  D DENNY-BROWN
Journal:  J Neurol Neurosurg Psychiatry       Date:  1951-11       Impact factor: 10.154

3.  Congenital sensory neuropathy.

Authors:  J E Barry; I J Hopkins; B W Neal
Journal:  Arch Dis Child       Date:  1974-02       Impact factor: 3.791

4.  Congenital sensory neuropathy.

Authors:  T J Murray
Journal:  Brain       Date:  1973-06       Impact factor: 13.501

5.  Histologic measurements and fine structure of biopsied sural nerve: normal, and in peroneal muscular atrophy, hypertrophic neuropathy, and congenital sensory neuropathy.

Authors:  P J Dyck
Journal:  Mayo Clin Proc       Date:  1966-11       Impact factor: 7.616
  5 in total
  1 in total

1.  Hereditary sensory neuropathy, a new type.

Authors:  A Staal; K Mechelse
Journal:  Hum Genet       Date:  1978-05-16       Impact factor: 4.132
  1 in total

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