Literature DB >> 7441268

Neurogenic scapuloperoneal syndrome in childhood.

R Mercelis, J Demeester, J J Martin.   

Abstract

Two brothers presented with a slowly progressive scapuloperoneal syndrome starting in early childhood. Initially there were myopathic EMG changes, but these changed to those of denervation. Neuromuscular biopsies at an interval of five years confirmed the neurogenic character of the muscle atrophy.

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Mesh：

Year:  1980        PMID： 7441268      PMCID： PMC490709          DOI： 10.1136/jnnp.43.10.888

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


  35 in total

1.  Scapuloperoneal atrophy with sensory involvement: Davidenkow's syndrome.

Authors:  M S Schwartz; M Swash
Journal:  J Neurol Neurosurg Psychiatry       Date:  1975-11       Impact factor: 10.154

2.  A neuromuscular syndrome of scapuloperoneal distribution.

Authors:  J A Feigenbaum; T L Munsat
Journal:  Bull Los Angeles Neurol Soc       Date:  1970-04

3.  [Scapulo-peroneal myopathies 14 cases including 8 with facial involvement].

Authors:  G Serratrice; H Roux; R Aquaron; D Gambarelli; J Baret
Journal:  Sem Hop       Date:  1969-10-26

4.  Scapuloperoneal dystrophy associated with neurogenic changes.

Authors:  K Takahashi; H Nakamura; R Nakashima
Journal:  J Neurol Sci       Date:  1974-12       Impact factor: 3.181

5.  [A new kinship with X-chromosomal benign progressive muscular dystrophy and early contractures (Emery-Dreifuss)].

Authors:  R Cammann; T Vehreschild; K Ernst
Journal:  Psychiatr Neurol Med Psychol (Leipz)       Date:  1974-07

6.  The neurogenic scapulo-peroneal syndrome.

Authors:  K Ricker; H G Mertens; K Schimrigk
Journal:  Eur Neurol       Date:  1968       Impact factor: 1.710

7.  A spinal muscular atrophy with scapuloperoneal distribution.

Authors:  E S Emery; G M Fenichel; G Eng
Journal:  Arch Neurol       Date:  1968-02

8.  Scapuloperoneal dystrophy and scapuloperoneal atrophy.

Authors:  H Zellweger; W F McCormick
Journal:  Helv Paediatr Acta       Date:  1968-12

9.  Quantitative histological and neurophysiological studies in scapulo-peroneal syndrome.

Authors:  G Scarlato; G Valli; M Bracchi
Journal:  Acta Neurol (Napoli)       Date:  1978-08

10.  Unusual type of benign x-linked muscular dystrophy.

Authors:  A E Emery; F E Dreifuss
Journal:  J Neurol Neurosurg Psychiatry       Date:  1966-08       Impact factor: 10.154
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  4 in total

1.  Familial autosomal recessive rigid spine syndrome with neurogenic facio-scapulo-peroneal muscle atrophy.

Authors:  L Palmucci; T Mongini; C Doriguzzi; M Maniscalco; D Schiffer
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-01       Impact factor: 10.154

2.  Scapuloperoneal syndrome with cardiomyopathy: report of a family with autosomal dominant inheritance and unusual features.

Authors:  A Chakrabarti; J M Pearce
Journal:  J Neurol Neurosurg Psychiatry       Date:  1981-12       Impact factor: 10.154

3.  Adult onset scapuloperoneal myopathy: diagnostic value of nerve morphometry and multiple muscle biopsies.

Authors:  W C Yee; A F Hahn; J J Gilbert
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-06       Impact factor: 10.154

4.  Autosomal dominant Emery-Dreifuss syndrome: evidence of a neurogenic variant of the disease.

Authors:  T N Witt; C G Garner; D Pongratz; X Baur
Journal:  Eur Arch Psychiatry Neurol Sci       Date:  1988
  4 in total

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