Literature DB >> 9598725

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

M C Speer1, 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.   

Abstract

Anticipation, an increase in severity or decrease in age of onset (AO) inherent in the transmission of the disease gene from affected parent to affected child, has been increasingly described in human disease. To assess anticipation in a large kindred in which autosomal dominant limb-girdle muscular dystrophy (LGMD1A) is segregating, age of disease onset was collected from patient interviews of affected family members. A total of 25 parent-offspring pairs, in which the parents are three (3R), four (4R), or five (5R) generations removed from a common founding ancestor, were available for analysis. Life table analyses showed significant decreases in age at first reported symptoms in the offspring of the 3R (chi2=5.55, p=0.02) and 4R (chi2=7.81, p=0.005) parents. Pairwise analyses confirmed this decrease with a median decrease of 13 years in transmission to offspring from 3R parents and 18 years in transmission to offspring from 4R parents. The finding of anticipation in this pedigree suggests that the mutation in LGMD1A may be the result of the expansion of an unstable trinucleotide repeat.

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Year:  1998        PMID: 9598725      PMCID: PMC1051279          DOI: 10.1136/jmg.35.4.305

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  8 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.  Adult-onset autosomal dominant limb-girdle muscular dystrophy.

Authors:  J G Chutkow; R R Heffner; A A Kramer; J A Edwards
Journal:  Ann Neurol       Date:  1986-08       Impact factor: 10.422

3.  Anticipation in myotonic dystrophy: new light on an old problem.

Authors:  P S Harper; H G Harley; W Reardon; D J Shaw
Journal:  Am J Hum Genet       Date:  1992-07       Impact factor: 11.025

4.  CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1.

Authors:  Y Kawaguchi; T Okamoto; M Taniwaki; M Aizawa; M Inoue; S Katayama; H Kawakami; S Nakamura; M Nishimura; I Akiguchi
Journal:  Nat Genet       Date:  1994-11       Impact factor: 38.330

5.  Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.

Authors:  M Mahadevan; C Tsilfidis; L Sabourin; G Shutler; C Amemiya; G Jansen; C Neville; M Narang; J Barceló; K O'Hoy
Journal:  Science       Date:  1992-03-06       Impact factor: 47.728

6.  Anticipation in bipolar affective disorder.

Authors:  M G McInnis; F J McMahon; G A Chase; S G Simpson; C A Ross; J R DePaulo
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

7.  Strategies for multilocus linkage analysis in humans.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

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

Authors:  J M Gilchrist; M Pericak-Vance; L Silverman; A D Roses
Journal:  Neurology       Date:  1988-01       Impact factor: 9.910

  8 in total
  3 in total

1.  A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A).

Authors:  Peter Reilich; Sabine Krause; Nicolai Schramm; Ursula Klutzny; Stefanie Bulst; Barbara Zehetmayer; Peter Schneiderat; Maggie C Walter; Benedikt Schoser; Hanns Lochmüller
Journal:  J Neurol       Date:  2011-02-20       Impact factor: 4.849

2.  Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: clinical description and gene localization to 5q31.

Authors:  H Feit; A Silbergleit; L B Schneider; J A Gutierrez; R P Fitoussi; C Réyès; G A Rouleau; B Brais; C E Jackson; J S Beckmann; E Seboun
Journal:  Am J Hum Genet       Date:  1998-12       Impact factor: 11.025

3.  Satellog: a database for the identification and prioritization of satellite repeats in disease association studies.

Authors:  Perseus I Missirlis; Carri-Lyn R Mead; Stefanie L Butland; B F Francis Ouellette; Rebecca S Devon; Blair R Leavitt; Robert A Holt
Journal:  BMC Bioinformatics       Date:  2005-06-10       Impact factor: 3.169

  3 in total

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