Literature DB >> 8482956

Congenital cervical spinal muscular atrophy: a non-familial, non progressive condition of the upper limbs.

G Hageman1, V T Ramaekers, B G Hilhorst, A R Rozeboom.   

Abstract

Two patients with congenital cervical spinal muscular atrophy had symmetrical severe muscle weakness and wasting confined to the upper limbs, areflexia and congenital contractures. The shoulders were internally rotated, elbows extended and wrists flexed. There were no sensory or bulbar symptoms, scoliosis, long tract signs or lower limb involvement. This condition should be regarded as a neurogenic type of arthrogryposis, limited to the upper limbs.

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Year:  1993        PMID： 8482956      PMCID： PMC1014952          DOI： 10.1136/jnnp.56.4.365

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


  13 in total

1.  World Federation of Neurology Research Committee Research Group on Neuromuscular Diseases.

Authors: 
Journal:  J Neurol Sci       Date:  1988-09       Impact factor: 3.181

2.  Electromyographic and histopathologic correlations in arthrogryposis.

Authors:  L D Amick; W W Johnson; H L Smith
Journal:  Arch Neurol       Date:  1967-05

3.  Segmental spinal muscular atrophy and dermatological findings in a patient with chromosome 18q deletion.

Authors:  B J Weiss; J Kamholz; A Ritter; E H Zackai; D M McDonald-McGinn; B Emanuel; K H Fischbeck
Journal:  Ann Neurol       Date:  1991-09       Impact factor: 10.422

4.  A dominantly inherited lower motor neuron disorder presenting at birth with associated arthrogryposis.

Authors:  P Fleury; G Hageman
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-10       Impact factor: 10.154

5.  The diagnostic management of newborns with congenital contractures: a nosologic study of 75 cases.

Authors:  G Hageman; E P Ippel; F A Beemer; J M de Pater; D Lindhout; J Willemse
Journal:  Am J Med Genet       Date:  1988-08

6.  Non familial juvenile distal spinal muscular atrophy of upper extremity.

Authors:  J B Peiris; K N Seneviratne; H R Wickremasinghe; S B Gunatilake; R Gamage
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-03       Impact factor: 10.154

7.  Neuropathologic findings in the spinal cords of 10 infants with arthrogryposis.

Authors:  S K Clarren; J G Hall
Journal:  J Neurol Sci       Date:  1983-01       Impact factor: 3.181

8.  The pathophysiology of arthrogryposis multiplex congenita neurologica.

Authors:  L M Brown; M J Robson; W J Sharrard
Journal:  J Bone Joint Surg Br       Date:  1980-08

9.  Congenital cervical spinal atrophy.

Authors:  H Darwish; H Sarnat; C Archer; K Brownell; S Kotagal
Journal:  Muscle Nerve       Date:  1981 Mar-Apr       Impact factor: 3.217

10.  Arthrogryposis multiplex congenita: spectrum of pathologic changes.

Authors:  B Q Banker
Journal:  Hum Pathol       Date:  1986-07       Impact factor: 3.466
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  2 in total

1.  A case of congenital bilateral absence of elbow flexor muscles: review of differential diagnosis and treatment.

Authors:  David T Netscher; Oluseyi Aliu; Saleh Samra; Eric Lewis
Journal:  Hand (N Y)       Date:  2007-10-09

2.  A novel Xp11.22-22.33 deletion suggesting a possible mechanism of congenital cervical spinal muscular atrophy.

Authors:  Jingwei Liu; Kelai Wang; Baomin Li; Xiaofan Yang
Journal:  Mol Genet Genomic Med       Date:  2021-01-29       Impact factor: 2.183
  2 in total

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