Literature DB >> 8989557

Maternal origin of inv dup(15) chromosomes in infantile autism.

T Martinsson1, T Johannesson, M Vujic, A Sjöstedt, S Steffenburg, C Gillberg, J Wahlström.   

Abstract

Six male patients with infantile autism and an extra inverted duplicated chromosome 15[inv dup(15)] were reported in a previous study. These patients had four copies of the chromosome region 15pter-q13, or an inv dup(15)(pter-->q13; q13-->pter). In this new study, DNA from the families of four of the patients were analysed using Southern based RFLPs and microsatellite polymorphisms from the region. In all four cases the inv dup(15) chromosome was of maternal origin. Furthermore, the data suggests that it originated in the maternal meiotic process rather than in an early mitosis in the developmental process of the embryo. The extra chromosome contained material from both of the maternally derived 15-chromosomes. Based on the molecular data presented here, a model for the origin of chromosome markers of this type is proposed.

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Year:  1996        PMID: 8989557     DOI: 10.1007/bf00538845

Source DB:  PubMed          Journal:  Eur Child Adolesc Psychiatry        ISSN: 1018-8827            Impact factor:   4.785


  26 in total

1.  Replication error, a new hypothesis to explain the origin of a supernumerary marker chromosome in a mentally retarded boy.

Authors:  A Wik Sjöstedt; M Alatalo; J Wahlström; U von Döbeln; R Olegård
Journal:  Hereditas       Date:  1989       Impact factor: 3.271

2.  Autism associated with marker chromosome.

Authors:  C Gillberg; S Steffenburg; J Wahlström; I C Gillberg; A Sjöstedt; T Martinsson; S Liedgren; O Eeg-Olofsson
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  1991-05       Impact factor: 8.829

3.  Identification of a marker chromosome as inv dup(15) by molecular analysis.

Authors:  Y Shibuya; H Tonoki; N Kajii; N Niikawa
Journal:  Clin Genet       Date:  1991-09       Impact factor: 4.438

4.  Prader-Willi syndrome and a bisatellited derivative of chromosome 15.

Authors:  L P Wisniewski; M E Witt; F Ginsberg-Fellner; J Wilner; R J Desnick
Journal:  Clin Genet       Date:  1980-07       Impact factor: 4.438

5.  Autism in Angelman syndrome: a population-based study.

Authors:  S Steffenburg; C L Gillberg; U Steffenburg; M Kyllerman
Journal:  Pediatr Neurol       Date:  1996-02       Impact factor: 3.372

6.  Cytogenetic and clinical studies in five cases of inv dup(15).

Authors:  L Wisniewski; T Hassold; J Heffelfinger; J V Higgins
Journal:  Hum Genet       Date:  1979-09       Impact factor: 4.132

7.  An extra idic(15p)(q11) chromosome in Prader-Willi syndrome.

Authors:  H Fujita; Y Sakamoto; Y Hamamoto
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

8.  Chromosome 15 uniparental disomy is not frequent in Angelman syndrome.

Authors:  J H Knoll; K A Glatt; R D Nicholls; S Malcolm; M Lalande
Journal:  Am J Hum Genet       Date:  1991-01       Impact factor: 11.025

9.  Clinical and molecular analysis of five inv dup(15) patients.

Authors:  W P Robinson; F Binkert; R Giné; C Vazquez; W Müller; W Rosenkranz; A Schinzel
Journal:  Eur J Hum Genet       Date:  1993       Impact factor: 4.246

10.  Parental origin of chromosome 15 deletion in Prader-Willi syndrome.

Authors:  M G Butler; C G Palmer
Journal:  Lancet       Date:  1983-06-04       Impact factor: 79.321

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  5 in total

1.  Autistic spectrum disorder associated with partial duplication of chromosome 15; three case reports.

Authors:  Mima Simic; Jeremy Turk
Journal:  Eur Child Adolesc Psychiatry       Date:  2004-12       Impact factor: 4.785

Review 2.  Chromosomal disorders and autism.

Authors:  C Gillberg
Journal:  J Autism Dev Disord       Date:  1998-10

3.  Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers.

Authors:  E H Cook; R Y Courchesne; N J Cox; C Lord; D Gonen; S J Guter; A Lincoln; K Nix; R Haas; B L Leventhal; E Courchesne
Journal:  Am J Hum Genet       Date:  1998-05       Impact factor: 11.025

4.  Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity.

Authors:  S E Roberts; F Maggouta; N S Thomas; P A Jacobs; J A Crolla
Journal:  Am J Hum Genet       Date:  2003-10-14       Impact factor: 11.025

5.  Medical conditions in autism spectrum disorders.

Authors:  Patrick F Bolton
Journal:  J Neurodev Disord       Date:  2009-07-07       Impact factor: 4.025

  5 in total

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