Literature DB >> 16059655

[Hereditary motor and sensory neuropathy (HMSN) with hypertrophy of the cauda equina and concomitant demyelinating white matter lesions].

B B Ertl-Wagner1, C Helmchen, A Stäbler, F Fassmann, M F Reiser.   

Abstract

Hereditary motor and sensory neuropathy (HMSN) is thought to almost exclusively affect the peripheral nervous system. We report the case of a 48-year-old patient with a longstanding history of HMSN type I who developed signs and symptoms of a cauda equina compression and of a central nervous system relapsing-remitting demyelinating white matter disease. Gross enlargement of the cauda equina fibers was detected by MR imaging of the lumbar spine. Cranial MR imaging revealed demyelinating white matter lesions. This case suggests that peripheral neuropathic mechanisms may also affect the central myelin in HMSN type I.

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Year:  2005        PMID: 16059655     DOI: 10.1007/s00117-003-0967-7

Source DB:  PubMed          Journal:  Radiologe        ISSN: 0033-832X            Impact factor:   0.635


  18 in total

1.  Is there room for MR imaging in the assessment of hereditary motor and sensory neuropathies?

Authors:  M Filippi
Journal:  AJNR Am J Neuroradiol       Date:  2000 Nov-Dec       Impact factor: 3.825

Review 2.  Hypertrophied cauda equina presenting as intradural mass: case report and review of literature.

Authors:  M Hahn; A Hirschfeld; H Sander
Journal:  Surg Neurol       Date:  1998-05

3.  Myelographic evidence for nerve root enlargement in a case of Charcot-Marie-Tooth disease.

Authors:  M Kremenitzer; P J Ager; L H Zingesser
Journal:  Neuroradiology       Date:  1976-07-30       Impact factor: 2.804

4.  Nerve root enlargement in Charcot-Marie-Tooth disease: CT appearance.

Authors:  J U Morano; W F Russell
Journal:  Radiology       Date:  1986-12       Impact factor: 11.105

5.  MR imaging of the cauda equina in hereditary motor sensory neuropathies: correlations with sural nerve biopsy.

Authors:  M Cellerini; S Salti; V Desideri; G Marconi
Journal:  AJNR Am J Neuroradiol       Date:  2000 Nov-Dec       Impact factor: 3.825

6.  Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene.

Authors:  K Hayasaka; M Himoro; W Sato; G Takada; K Uyemura; N Shimizu; T D Bird; P M Conneally; P F Chance
Journal:  Nat Genet       Date:  1993-09       Impact factor: 38.330

Review 7.  Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies.

Authors:  E Nelis; N Haites; C Van Broeckhoven
Journal:  Hum Mutat       Date:  1999       Impact factor: 4.878

8.  Transient central nervous system white matter abnormality in X-linked Charcot-Marie-Tooth disease.

Authors:  Henry L Paulson; James Y Garbern; Timothy F Hoban; Karen M Krajewski; Richard A Lewis; Kenneth H Fischbeck; Robert I Grossman; Robert Lenkinski; John A Kamholz; Michael E Shy
Journal:  Ann Neurol       Date:  2002-10       Impact factor: 10.422

9.  Compression syndromes due to hypertrophic nerve roots in hereditary motor sensory neuropathy type I.

Authors:  S A Rosen; H Wang; D R Cornblath; S Uematsu; O Hurko
Journal:  Neurology       Date:  1989-09       Impact factor: 9.910

10.  Hereditary neuropathy with liability to pressure palsies: assocation with central nervous system demyelination.

Authors:  A A Amato; R J Barohn
Journal:  Muscle Nerve       Date:  1996-06       Impact factor: 3.217

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