Literature DB >> 9032642

No evidence for uniparental disomy as a common cause of Sotos syndrome.

M Smith1, P Fullwood, Y Qi, S Palmer, M Upadhyaya, T Cole.   

Abstract

A number of rare diseases (including Sotos syndrome) of unknown aetiology, which occur mainly sporadically and with features of growth disorder and developmental delay, may be caused by imprinted genes and therefore be associated with UPD. Using 112 dinucleotide repeat DNA polymorphisms, we have examined parental inheritance of all autosome pairs, except chromosome 15, in 29 patients with Sotos syndrome. All informative cases showed biparental inheritance and no cases of UPD were found. We conclude that Sotos syndrome is either not caused by an imprinted gene or that UPD is rare or of a segmental form in its aetiology.

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Year:  1997        PMID: 9032642      PMCID: PMC1050839          DOI: 10.1136/jmg.34.1.10

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


  19 in total

1.  Linkage mapping of the highly informative DNA marker D21S156 to human chromosome 21 using a polymorphic GT dinucleotide repeat.

Authors:  J G Lewis; J L Weber; M B Petersen; S A Slaugenhaupt; A Kwitek; P E May; A C Warren; A Chakravarti; S E Antonarakis
Journal:  Genomics       Date:  1990-10       Impact factor: 5.736

2.  Sotos syndrome and de novo balanced autosomal translocation (t(3;6)(p21;p21))

Authors:  C T Schrander-Stumpel; J P Fryns; G G Hamers
Journal:  Clin Genet       Date:  1990-03       Impact factor: 4.438

3.  Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

Authors:  L M Kunkel; K D Smith; S H Boyer; D S Borgaonkar; S S Wachtel; O J Miller; W R Breg; H W Jones; J M Rary
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

Review 4.  Parental imprinting of autosomal mammalian genes.

Authors:  A Efstratiadis
Journal:  Curr Opin Genet Dev       Date:  1994-04       Impact factor: 5.578

Review 5.  Beckwith-Wiedemann syndrome.

Authors:  M Elliott; E R Maher
Journal:  J Med Genet       Date:  1994-07       Impact factor: 6.318

Review 6.  Genetic imprinting in clinical genetics.

Authors:  A Clarke
Journal:  Dev Suppl       Date:  1990

7.  A new genetic concept: uniparental disomy and its potential effect, isodisomy.

Authors:  E Engel
Journal:  Am J Med Genet       Date:  1980

8.  Differential activity of maternally and paternally derived chromosome regions in mice.

Authors:  B M Cattanach; M Kirk
Journal:  Nature       Date:  1985 Jun 6-12       Impact factor: 49.962

9.  Cerebral gigantism (Sotos syndrome) in two patients with fra(X) chromosomes.

Authors:  F A Beemer; H Veenema; J M de Pater
Journal:  Am J Med Genet       Date:  1986 Jan-Feb

10.  Uniparental disomy as a mechanism for human genetic disease.

Authors:  J E Spence; R G Perciaccante; G M Greig; H F Willard; D H Ledbetter; J F Hejtmancik; M S Pollack; W E O'Brien; A L Beaudet
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

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  2 in total

1.  Diagnosing Friedreich's ataxia.

Authors:  N W Wood
Journal:  Arch Dis Child       Date:  1998-03       Impact factor: 3.791

2.  Growing interest in overgrowth.

Authors:  T Cole
Journal:  Arch Dis Child       Date:  1998-03       Impact factor: 3.791

  2 in total

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