Literature DB >> 8933228

A newly-described myotonic disorder (proximal myotonic myopathy--PROMM): personal experience and review of the literature.

G Meola1, V Sansone.   

Abstract

The aim of this study is to describe the essential characteristics of a family affected by the newly-described proximal myotonic myopathy (PROMM) The clinical, laboratory and genetic findings are described and compared with those reported in the literature, and the clinical spectrum of the manifestations that are similar to but distinct from myotonic dystrophy (MD) is also explored. This has practical implications because the cases so far described suggest that the long-term prognosis with PROMM seems to be more favourable than that of patients with MD.

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Year:  1996        PMID: 8933228     DOI: 10.1007/bf01999897

Source DB:  PubMed          Journal:  Ital J Neurol Sci        ISSN: 0392-0461


  25 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.  Proximal weakness as the primary manifestation of myotonic dystrophy in older adults.

Authors:  D Lacomis; D A Chad; T W Smith
Journal:  Muscle Nerve       Date:  1994-06       Impact factor: 3.217

Review 3.  Proximal myotonic myopathy: mini-review of a recently delineated clinical disorder.

Authors:  R T MOxley
Journal:  Neuromuscul Disord       Date:  1996-03       Impact factor: 4.296

4.  Myotonic dystrophy: correlation of clinical symptoms with the size of the CTG trinucleotide repeat.

Authors:  A Jaspert; R Fahsold; H Grehl; D Claus
Journal:  J Neurol       Date:  1995-01       Impact factor: 4.849

5.  Anticipation in myotonic dystrophy. I. Statistical verification based on clinical and haplotype findings.

Authors:  T Ashizawa; C J Dunne; J R Dubel; M B Perryman; H F Epstein; E Boerwinkle; J F Hejtmancik
Journal:  Neurology       Date:  1992-10       Impact factor: 9.910

6.  A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies.

Authors:  G Meola; V Sansone; S Radice; S Skradski; L Ptacek
Journal:  Neuromuscul Disord       Date:  1996-05       Impact factor: 4.296

7.  Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy.

Authors:  J Buxton; P Shelbourne; J Davies; C Jones; T Van Tongeren; C Aslanidis; P de Jong; G Jansen; M Anvret; B Riley
Journal:  Nature       Date:  1992-02-06       Impact factor: 49.962

8.  Mutation in the S4 segment of the adult skeletal sodium channel gene in an Italian paramyotonia congenita (PC) family.

Authors:  V Sansone; G Rotondo; L J Ptacek; G Meola
Journal:  Ital J Neurol Sci       Date:  1994-12

9.  Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita.

Authors:  L J Ptácek; A L George; R L Barchi; R C Griggs; J E Riggs; M Robertson; M F Leppert
Journal:  Neuron       Date:  1992-05       Impact factor: 17.173

10.  Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy.

Authors:  H G Harley; S A Rundle; J C MacMillan; J Myring; J D Brook; S Crow; W Reardon; I Fenton; D J Shaw; P S Harper
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

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  2 in total

1.  Validation of sensitivity and specificity of tetraplet-primed PCR (TP-PCR) in the molecular diagnosis of myotonic dystrophy type 2 (DM2).

Authors:  Claudio Catalli; Alessandra Morgante; Raniero Iraci; Fabrizio Rinaldi; Annalisa Botta; Giuseppe Novelli
Journal:  J Mol Diagn       Date:  2010-07-08       Impact factor: 5.568

2.  A case of myotonic dystrophy with pigmentary retinal changes.

Authors:  Ungsoo Samuel Kim; Ji Soo Kim; Jeong-Min Hwang
Journal:  Korean J Ophthalmol       Date:  2009-06-09
  2 in total

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