Literature DB >> 3091775

Congenital muscular dystrophy and cerebral CT scan anomalies. Results of a collaborative study of the Société de Neurologie Infantile.

B Echenne, M Arthuis, C Billard, J Campos-Castello, Y Castel, O Dulac, D Fontan, A Gauthier, S Kulakowski, G De Meuron.   

Abstract

We present the results of a collaborative study on the association of congenital muscular dystrophy with central nervous system anomalies revealed by CT scan investigation of 10 patients. In seven children, an abnormal hypodensity of the cerebral white matter is found; in four of these patients, this radiological anomaly is either isolated, or associated with a moderate intellectual impairment; in one case, severe mental retardation and ocular changes had occurred; in the other two cases, the muscular disease was progressing slowly, in association with microcephaly, epilepsy, and moderate mental retardation. Three children were afflicted with a severe early encephalopathy and congenital muscular dystrophy, and presented signs of cortical and subcortical atrophy on CT scan. Two of these patients corresponded to different types of cerebro-ocular dysplasia-muscular dystrophy syndromes, and the third patient of Fukuyama's congenital muscular dystrophy. These observations are discussed and compared with those reported in the literature. The authors emphasize the need to investigate possible cerebral CT scan anomalies in congenital muscular dystrophies, and to look for muscular changes in some prenatal encephalopathies.

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Year:  1986        PMID: 3091775     DOI: 10.1016/0022-510x(86)90046-8

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  10 in total

1.  Occidental type cerebromuscular dystrophy: a report of eleven cases.

Authors:  H Topaloğlu; K Yalaz; Y Renda; M Cağlar; S Göğüs; G Kale; K Gücüyener; G Nurlu
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-03       Impact factor: 10.154

2.  Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy.

Authors:  I S Naom; M D'Alessandro; H Topaloglu; C Sewry; A Ferlini; A Helbling-Leclerc; P Guicheney; J Weissenbach; K Schwartz; K Bushby; J Philpot; V Dubowitz; F Muntoni
Journal:  J Med Genet       Date:  1997-02       Impact factor: 6.318

3.  Pattern recognition in magnetic resonance imaging of white matter disorders in children and young adults.

Authors:  M S van der Knaap; J Valk; N de Neeling; J J Nauta
Journal:  Neuroradiology       Date:  1991       Impact factor: 2.804

4.  Serial MRI in Fukuyama type congenital muscular dystrophy.

Authors:  M Aihara; Y Tanabe; K Kato
Journal:  Neuroradiology       Date:  1992       Impact factor: 2.804

5.  Congenital muscular dystrophy. A study on the variability of morphological changes and dystrophin distribution in muscle biopsies.

Authors:  Q H Leyten; H J ter Laak; F J Gabreëls; W O Renier; K Renkawek; R C Sengers
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

6.  Congenital muscular dystrophy, brain and eye abnormalities: one or more clinical entities?

Authors:  A M Laverda; M A Battaglia; P Drigo; P A Battistella; G L Casara; A Suppiej; R Casellato
Journal:  Childs Nerv Syst       Date:  1993-04       Impact factor: 1.475

7.  Congenital muscular dystrophy and cerebellar vermis agenesis in two brothers.

Authors:  O Arancio; L G Bongiovanni; G Bonadonna; G Tomelleri; D De Grandis
Journal:  Ital J Neurol Sci       Date:  1988-10

8.  Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping.

Authors:  B Cormand; K Avela; H Pihko; P Santavuori; B Talim; H Topaloglu; A de la Chapelle; A E Lehesjoki
Journal:  Am J Hum Genet       Date:  1999-01       Impact factor: 11.025

9.  Brain alterations in the classical form of congenital muscular dystrophy. Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle.

Authors:  C P Trevisan; F Martinello; E Ferruzza; M Fanin; M Chevallay; F M Tomé
Journal:  Childs Nerv Syst       Date:  1996-10       Impact factor: 1.475

10.  Congenital muscular dystrophy: brain alterations in an unselected series of Western patients.

Authors:  C P Trevisan; C Carollo; P Segalla; C Angelini; P Drigo; R Giordano
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-04       Impact factor: 10.154

  10 in total

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