Literature DB >> 7207500

Congenital cervical spinal atrophy.

H Darwish, H Sarnat, C Archer, K Brownell, S Kotagal.   

Abstract

Three children presented at birth with axial hypotonia and symmetrical flaccid paresis limited to the upper extremities, and involving proximal and distal muscle groups. At birth, palmar flexion creases were poorly developed, and the hand muscles were atrophic. These clinical features, the muscle biopsy findings, and the nonprogressive course, suggest a vascular insult to the cervical spinal cord during gestation. The term, congenital cervical spinal atrophy seems most descriptive of these features.

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Mesh:

Year:  1981        PMID: 7207500     DOI: 10.1002/mus.880040205

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  4 in total

1.  A predominantly cervical form of spinal muscular atrophy.

Authors:  K Yalaz; H Topaloglu; M Aksu; K Gucuyener; M Topcu
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-06       Impact factor: 10.154

2.  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

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

Authors:  G Hageman; V T Ramaekers; B G Hilhorst; A R Rozeboom
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-04       Impact factor: 10.154

4.  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

  4 in total

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