Literature DB >> 26835328

Uniparental disomy in Robertsonian translocations: strategies for uniparental disomy testing.

Moh-Ying Yip1.   

Abstract

Robertsonian translocations (ROBs) are whole arm rearrangements involving the acrocentric chromosomes 13-15 and 21-22 and carriers are at increased risk for aneuploidy and thus uniparental disomy (UPD). Chromosomes 14 and 15 are imprinted with expression of genes dependent on the parental origin of the chromosome. Correction of a trisomic or monosomic conceptus for chromosomes 14 or 15 would lead to one of the established UPD 14mat/pat or UPD 15 (Prader-Willi/Angelman) syndromes (PWS/AS). In view of this, prenatal UPD testing should be considered for balanced carriers of a ROB, fetuses with a familial or de novo balanced ROB that contains chromosome 14 or 15 or with a normal karyotype when a parent is a carrier of a balanced ROB with a 14 or 15. Individuals with congenital anomalies and an abnormal phenotype and carry a ROB involving the two imprinted chromosomes should also be UPD tested.

Entities:  

Keywords:  Imprinting; Robertsonian translocations (ROBs); isochromosome; trisomy rescue; uniparental disomy (UPD)

Year:  2014        PMID: 26835328      PMCID: PMC4729106          DOI: 10.3978/j.issn.2224-4336.2014.03.03

Source DB:  PubMed          Journal:  Transl Pediatr        ISSN: 2224-4336


  49 in total

Review 1.  Parental origin and timing of de novo Robertsonian translocation formation.

Authors:  Ruma Bandyopadhyay; Anita Heller; Cami Knox-DuBois; Christopher McCaskill; Sue Ann Berend; Scott L Page; Lisa G Shaffer
Journal:  Am J Hum Genet       Date:  2002-11-06       Impact factor: 11.025

2.  CCMG guidelines: prenatal and postnatal diagnostic testing for uniparental disomy.

Authors:  A J Dawson; J Chernos; J McGowan-Jordan; J Lavoie; S Shetty; M Steinraths; J-C Wang; J Xu
Journal:  Clin Genet       Date:  2010-10-12       Impact factor: 4.438

3.  Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations.

Authors:  Anna Ruggeri; Francesca Dulcetti; Monica Miozzo; Francesca R Grati; Beatrice Grimi; Silvano Bellato; Federica Natacci; Federico Maggi; Giuseppe Simoni
Journal:  Prenat Diagn       Date:  2004-12-15       Impact factor: 3.050

4.  Uniparental disomy 15 resulting from "correction" of an initial trisomy 15.

Authors:  S G Purvis-Smith; T Saville; S Manass; M Y Yip; P R Lam-Po-Tang; B Duffy; H Johnston; D Leigh; B McDonald
Journal:  Am J Hum Genet       Date:  1992-06       Impact factor: 11.025

5.  Chromosomal segregation in spermatozoa of 14 Robertsonian translocation carriers.

Authors:  Gonul Ogur; Elvire Van Assche; Walter Vegetti; Greta Verheyen; Herman Tournaye; Maryse Bonduelle; André Van Steirteghem; Inge Liebaers
Journal:  Mol Hum Reprod       Date:  2006-03-08       Impact factor: 4.025

6.  Distribution of aneuploidy in human gametes: comparison between human sperm and oocytes.

Authors:  R H Martin; E Ko; A Rademaker
Journal:  Am J Med Genet       Date:  1991-06-01

7.  Origin of uniparental disomy 15 in patients with Prader-Willi or Angelman syndrome.

Authors:  C Fridman; C P Koiffmann
Journal:  Am J Med Genet       Date:  2000-09-18

8.  Maternal uniparental disomy for chromosome 14.

Authors:  I K Temple; A Cockwell; T Hassold; D Pettay; P Jacobs
Journal:  J Med Genet       Date:  1991-08       Impact factor: 6.318

9.  UPD 13: no indication of maternal or paternal imprinting of genes on chromosome 13.

Authors:  H Slater; J H Shaw; A Bankier; S M Forrest; G Dawson
Journal:  J Med Genet       Date:  1995-06       Impact factor: 6.318

10.  Prenatal diagnosis of a homologous Robertsonian translocation involving chromosome 15.

Authors:  D J Abrams; A R Aronoff; S Ann Berend; B B Roa; L G Shaffer; M R Geier
Journal:  Prenat Diagn       Date:  2001-08       Impact factor: 3.050

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  7 in total

Review 1.  The dilemma of diagnostic testing for Prader-Willi syndrome.

Authors:  Arabella Smith; Dorothy Hung
Journal:  Transl Pediatr       Date:  2017-01

2.  Homozygosity for a Robertsonian Translocation (13q;14q) in a Phenotypically Normal 44, XX Female with a History of Recurrent Abortion and a Normal Pregnancy Outcome.

Authors:  Mohammad Miryounesi; Mehdi Diantpour; Elahe Motevaseli; Soudeh Ghafouri-Fard
Journal:  J Reprod Infertil       Date:  2016 Jul-Sep

3.  De novo Balanced Robertsonian Translocation rob(22;22)(q10;q10) in a Woman with Recurrent Pregnancy Loss: A Rare Case.

Authors:  Nawras Alhalabi; Walid Al-Achkar; Abdulsamad Wafa; Mazen Kenj; Marwan Alhalabi
Journal:  J Reprod Infertil       Date:  2018 Jan-Mar

4.  A rapid and accurate methylation-sensitive high-resolution melting analysis assay for the diagnosis of Prader Willi and Angelman patients.

Authors:  Igor Ribeiro Ferreira; Wilton Darleans Dos Santos Cunha; Leonardo Henrique Ferreira Gomes; Hiago Azevedo Cintra; Letícia Lopes Cabral Guimarães Fonseca; Elenice Ferreira Bastos; Juan Clinton Llerena; Zilton Farias Meira de Vasconcelos; Letícia da Cunha Guida
Journal:  Mol Genet Genomic Med       Date:  2019-04-29       Impact factor: 2.183

Review 5.  Genotype-Phenotype Relationships and Endocrine Findings in Prader-Willi Syndrome.

Authors:  Régis Afonso Costa; Igor Ribeiro Ferreira; Hiago Azevedo Cintra; Leonardo Henrique Ferreira Gomes; Letícia da Cunha Guida
Journal:  Front Endocrinol (Lausanne)       Date:  2019-12-13       Impact factor: 5.555

Review 6.  Prenatal Detection of Uniparental Disomies (UPD): Intended and Incidental Finding in the Era of Next Generation Genomics.

Authors:  Thomas Eggermann
Journal:  Genes (Basel)       Date:  2020-12-03       Impact factor: 4.096

7.  A Male Case of Kagami-Ogata Syndrome Caused by Paternal Unipaternal Disomy 14 as a Result of a Robertsonian Translocation.

Authors:  Xiaoxue Wang; Hui Pang; Birju A Shah; Hongcang Gu; Lijun Zhang; Hua Wang
Journal:  Front Pediatr       Date:  2020-03-10       Impact factor: 3.418

  7 in total

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