Literature DB >> 7585681

Myotonic dystrophy in a large Sicilian kinship: a case report.

R Trifiletti1, E Parano, R Falsaperla, G Incorpora.   

Abstract

A large Sicilian kinship in which myotonic dystrophy (DM) affected spanning four generations is presented. The pedigree clearly illustrates the phenomenon of anticipation, and illustrates that this phenomenon is more marked when transmission occurs through an affected female rather than an affected male. The pedigree is interpreted in light of recent genetic advances in DM. Neurosurgeons and neurologists should consider a diagnosis of DM when asked to evaluate a floppy infant with enlarged lateral ventricles, and should be aware of special features regarding its inheritance pattern.

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Year:  1995        PMID: 7585681     DOI: 10.1007/BF00334964

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  8 in total

1.  Central nervous system magnetic resonance imaging findings in myotonic dystrophy.

Authors:  R H Glantz; R B Wright; M S Huckman; D C Garron; I M Siegel
Journal:  Arch Neurol       Date:  1988-01

2.  Structure and genomic sequence of the myotonic dystrophy (DM kinase) gene.

Authors:  M S Mahadevan; C Amemiya; G Jansen; L Sabourin; S Baird; C E Neville; N Wormskamp; B Segers; M Batzer; J Lamerdin
Journal:  Hum Mol Genet       Date:  1993-03       Impact factor: 6.150

3.  The natural history of congenital myotonic dystrophy: mortality and long term clinical aspects.

Authors:  W Reardon; R Newcombe; I Fenton; J Sibert; P S Harper
Journal:  Arch Dis Child       Date:  1993-02       Impact factor: 3.791

4.  Cerebral ventricular dilation in congenital myotonic dystrophy.

Authors:  R Regev; L S de Vries; J Z Heckmatt; V Dubowitz
Journal:  J Pediatr       Date:  1987-09       Impact factor: 4.406

Review 5.  Congenital myotonic dystrophy; a report on thirteen cases and a review of the literature.

Authors:  A T Hageman; F J Gabreëls; K D Liem; K Renkawek; J M Boon
Journal:  J Neurol Sci       Date:  1993-03       Impact factor: 3.181

6.  The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy.

Authors:  A Hunter; C Tsilfidis; G Mettler; P Jacob; M Mahadevan; L Surh; R Korneluk
Journal:  J Med Genet       Date:  1992-11       Impact factor: 6.318

7.  Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy.

Authors:  H G Harley; J D Brook; S A Rundle; S Crow; W Reardon; A J Buckler; P S Harper; D E Housman; D J Shaw
Journal:  Nature       Date:  1992-02-06       Impact factor: 49.962

8.  Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy.

Authors:  C Tsilfidis; A E MacKenzie; G Mettler; J Barceló; R G Korneluk
Journal:  Nat Genet       Date:  1992-06       Impact factor: 38.330

  8 in total

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