Literature DB >> 7818265

Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome.

T Toda1, M Yoshioka, Y Nakahori, I Kanazawa, Y Nakamura, Y Nakagome.   

Abstract

Both Fukuyama-type congenital muscular dystrophy (FCMD) and Walker-Warburg syndrome (WWS) are unusual genetic syndromes consisting of congenital muscular dystrophy and complex malformations of the brain and eye. It has been intensively discussed whether FCMD and WWS belong to the same disease entity or not. We analyzed a family in which 3 siblings were affected with either FCMD or WWS by using polymorphic microsatellites flanking the FCMD locus on chromosome 9q31-33. The results suggested that both FCMD and WWS siblings shared the identical combination of mutations on either allele of the FCMD locus. FCMD and WWS could be "genetically" identical.

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Year:  1995        PMID: 7818265     DOI: 10.1002/ana.410370118

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  8 in total

1.  A novel pattern of oculocerebral malformation.

Authors:  B J Clark; W R Lee; D Doyle; R Arngrimsson; J L Tolmie; J B Stephenson
Journal:  Br J Ophthalmol       Date:  1997-06       Impact factor: 4.638

Review 2.  Syndromes with lissencephaly.

Authors:  D T Pilz; O W Quarrell
Journal:  J Med Genet       Date:  1996-04       Impact factor: 6.318

3.  Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration.

Authors:  H O Sweet; R T Bronson; K R Johnson; S A Cook; M T Davisson
Journal:  Mamm Genome       Date:  1996-11       Impact factor: 2.957

Review 4.  Investigation of muscle disease.

Authors:  F L Mastaglia; N G Laing
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-03       Impact factor: 10.154

Review 5.  Muscular dystrophies.

Authors:  V Kalra
Journal:  Indian J Pediatr       Date:  2000-12       Impact factor: 1.967

6.  Congenital muscular dystrophy with severe retrocollis and mental retardation: a report of two siblings.

Authors:  L Nashef; B D Lake; A H Schapira
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-03       Impact factor: 10.154

7.  Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb.

Authors:  T Toda; M Miyake; K Kobayashi; K Mizuno; K Saito; M Osawa; Y Nakamura; I Kanazawa; Y Nakagome; K Tokunaga; Y Nakahori
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

8.  Degree of Cajal-Retzius Cell Mislocalization Correlates with the Severity of Structural Brain Defects in Mouse Models of Dystroglycanopathy.

Authors:  Helen S Booler; Josie L Williams; Mark Hopkinson; Susan C Brown
Journal:  Brain Pathol       Date:  2015-10-12       Impact factor: 6.508

  8 in total

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