Literature DB >> 8434633

Decrease in the size of the myotonic dystrophy CTG repeat during transmission from parent to child: implications for genetic counselling and genetic anticipation.

A G Hunter1, P Jacob, K O'Hoy, I MacDonald, G Mettler, C Tsilfidis, R G Korneluk.   

Abstract

Recently an unstable trinucleotide CTG repeat, located within the 3' untranslated region of a gene on 19q13.3 was discovered in kindreds with myotonic dystrophy (DM). The age-of-onset/severity of DM shows a good correlation with CTG repeat size, and pedigrees and data reported to date have shown a striking trend toward amplification of the size of the CTG repeat during transmission from parent to child. The amplification has been accepted as the biological explanation for anticipation in the clinical severity observed in many families with DM. In this paper we report on 3 families where CTG amplification decreased during transmission from parent to child. In one case there was a gene conversion event, while in the remaining 2 there was a simpler reduction in the size of the repeat length. The changes appear to have been accompanied by a reduction in clinical severity in the child when compared to the parent. These observations are discussed in terms of their clinical implications and the biases that may exist in much of the reported data.

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Year:  1993        PMID: 8434633     DOI: 10.1002/ajmg.1320450330

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  8 in total

1.  Comparison of CTG repeat length expansion and clinical progression of myotonic dystrophy over a five year period.

Authors:  L Martorell; J M Martinez; N Carey; K Johnson; M Baiget
Journal:  J Med Genet       Date:  1995-08       Impact factor: 6.318

2.  Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM).

Authors:  H G Brunner; H T Brüggenwirth; W Nillesen; G Jansen; B C Hamel; R L Hoppe; C E de Die; C J Höweler; B A van Oost; B Wieringa
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

3.  Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 Brazilian families.

Authors:  M R Passos-Bueno; A Cerqueira; M Vainzof; S K Marie; M Zatz
Journal:  J Med Genet       Date:  1995-01       Impact factor: 6.318

4.  Possible anticipation associated with a novel splice site mutation in episodic ataxia type 2.

Authors:  Kwang-Dong Choi; Ji-Won Yook; Min-Ji Kim; Hyang-Sook Kim; Young-Eun Park; Ji Soo Kim; Jae-Hwan Choi; Jin-Hong Shin; Dae-Seong Kim
Journal:  Neurol Sci       Date:  2013-01-24       Impact factor: 3.307

5.  Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm.

Authors:  G Jansen; P Willems; M Coerwinkel; W Nillesen; H Smeets; L Vits; C Höweler; H Brunner; B Wieringa
Journal:  Am J Hum Genet       Date:  1994-04       Impact factor: 11.025

6.  The fragile X premutation in carriers and its effect on mutation size in offspring.

Authors:  G S Fisch; K Snow; S N Thibodeau; M Chalifaux; J J Holden; D L Nelson; P N Howard-Peebles; A Maddalena
Journal:  Am J Hum Genet       Date:  1995-05       Impact factor: 11.025

7.  Double-strand breaks in the myotonic dystrophy type 1 and the fragile X syndrome triplet repeat sequences induce different types of mutations in DNA flanking sequences in Escherichia coli.

Authors:  Beata Kosmider; Robert D Wells
Journal:  Nucleic Acids Res       Date:  2006-09-29       Impact factor: 16.971

8.  Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy.

Authors:  T Ashizawa; M Anvret; M Baiget; J M Barceló; H Brunner; A M Cobo; B Dallapiccola; R G Fenwick; U Grandell; H Harley
Journal:  Am J Hum Genet       Date:  1994-03       Impact factor: 11.025

  8 in total

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