Literature DB >> 3275904

Clinical and genetic investigation in autosomal dominant limb-girdle muscular dystrophy.

J M Gilchrist1, M Pericak-Vance, L Silverman, A D Roses.   

Abstract

Limb-girdle muscular dystrophy is a syndrome of progressive myopathic weakness affecting shoulder and hip girdle and proximal arm and leg muscles. The disease occurs either sporadically or inherited as an autosomal recessive trait. Autosomal dominant inheritance is rare. We report a large family with apparent autosomal dominant inheritance. Sixteen members were affected with a disease characterized by proximal weakness, leg greater than arm, onset in the third decade, elevated CK and CK MB levels, and myopathic EMGs and muscle biopsies. Linkage analysis revealed no conclusive linkage.

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Year:  1988        PMID: 3275904     DOI: 10.1212/wnl.38.1.5

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  19 in total

1.  Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q.

Authors:  M C Speer; L H Yamaoka; J H Gilchrist; C P Gaskell; J M Stajich; J M Vance; A Kazantsev; A A Lastra; C S Haynes; J S Beckmann
Journal:  Am J Hum Genet       Date:  1992-06       Impact factor: 11.025

2.  Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7.

Authors:  M C Speer; J M Vance; J M Grubber; F Lennon Graham; J M Stajich; K D Viles; A Rogala; R McMichael; J Chutkow; C Goldsmith; R W Tim; M A Pericak-Vance
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

3.  Evidence-based guideline summary: diagnosis and treatment of limb-girdle and distal dystrophies: report of the guideline development subcommittee of the American Academy of Neurology and the practice issues review panel of the American Association of Neuromuscular & Electrodiagnostic Medicine.

Authors:  Pushpa Narayanaswami; Michael Weiss; Duygu Selcen; William David; Elizabeth Raynor; Gregory Carter; Matthew Wicklund; Richard J Barohn; Erik Ensrud; Robert C Griggs; Gary Gronseth; Anthony A Amato
Journal:  Neurology       Date:  2014-10-14       Impact factor: 9.910

4.  Evidence for anticipation in autosomal dominant limb-girdle muscular dystrophy.

Authors:  M C Speer; J M Gilchrist; J M Stajich; P C Gaskell; C A Westbrook; S K Horrigan; L Bartoloni; L H Yamaoka; W K Scott; M A Pericak-Vance
Journal:  J Med Genet       Date:  1998-04       Impact factor: 6.318

5.  Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21.

Authors:  A J van der Kooi; M van Meegen; T M Ledderhof; E M McNally; M de Visser; P A Bolhuis
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

Review 6.  Myofibrillar myopathies.

Authors:  Duygu Selcen
Journal:  Neuromuscul Disord       Date:  2011-01-20       Impact factor: 4.296

7.  Abnormal dystrophin expression in patients with limb girdle syndromes.

Authors:  S Beyenburg; S Zierz; K Arahata; R R Mundegar; W Friedl; F Jerusalem
Journal:  J Neurol       Date:  1994-02       Impact factor: 4.849

Review 8.  [Limb girdle muscular dystrophies].

Authors:  J Finsterer
Journal:  Nervenarzt       Date:  2004-12       Impact factor: 1.214

9.  Myotonic dystrophy and limb girdle muscular dystrophy in one family.

Authors:  R Schröder; S Beyenburg; J Weber; K Olek; S Zierz
Journal:  Clin Investig       Date:  1994-05

10.  Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.

Authors:  M C Speer; J M Gilchrist; J G Chutkow; R McMichael; C A Westbrook; J M Stajich; E M Jorgenson; P C Gaskell; B L Rosi; R Ramesar
Journal:  Am J Hum Genet       Date:  1995-12       Impact factor: 11.025

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