Literature DB >> 25547535

Mosaicism and uniparental disomy in prenatal diagnosis.

Thomas Eggermann1, Lukas Soellner2, Karin Buiting3, Dieter Kotzot4.   

Abstract

Chromosomal mosaicism is the presence of numerous cell lines with different chromosomal complements in the same individual. Uniparental disomy (UPD) is the inheritance of two homologous chromosomes from the same parent. These genetic anomalies arise from errors in meiosis and/or mitosis and can occur independently or in combination. Due to the formation mechanisms of UPD, low-level or undetected mosaicisms are assumed for a significant number of UPD cases. The pre- and postnatal clinical consequences of mosaicism for chromosomal aberrations and/or UPD depend on the gene content of the involved chromosome. In prenatal evaluation of chromosomal mosaicism and UPD, genetic counseling should be offered before any laboratory testing.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  aneuploidy; genetic counseling; genetic testing; mosaicism; prenatal diagnosis; uniparental disomy

Mesh:

Year:  2014        PMID: 25547535     DOI: 10.1016/j.molmed.2014.11.010

Source DB:  PubMed          Journal:  Trends Mol Med        ISSN: 1471-4914            Impact factor:   11.951


  31 in total

Review 1.  Uniparental disomy as an unexpected cause of Meckel-Gruber syndrome: report of a case.

Authors:  Nadia Ortiz Bruechle; Peter Steuernagel; Klaus Zerres; Ingo Kurth; Thomas Eggermann; Cordula Knopp
Journal:  Pediatr Nephrol       Date:  2017-06-15       Impact factor: 3.714

Review 2.  Mosaicism in Preimplantation Human Embryos: When Chromosomal Abnormalities Are the Norm.

Authors:  Rajiv C McCoy
Journal:  Trends Genet       Date:  2017-04-28       Impact factor: 11.639

3.  Prenatal Diagnosis of Chromosomal Mosaicism in Over 18,000 Pregnancies: A Five-Year Single-Tertiary-Center Retrospective Analysis.

Authors:  Shuyuan Li; Yiru Shi; Xu Han; Yiyao Chen; Yinghua Shen; Wenjing Hu; Xinrong Zhao; Yanlin Wang
Journal:  Front Genet       Date:  2022-05-16       Impact factor: 4.772

Review 4.  Imprinted Genes Impact Upon Beta Cell Function in the Current (and Potentially Next) Generation.

Authors:  Chelsie Villanueva-Hayes; Steven J Millership
Journal:  Front Endocrinol (Lausanne)       Date:  2021-04-27       Impact factor: 5.555

5.  Birth of a child with trisomy 9 mosaicism syndrome associated with paternal isodisomy 9: case of a positive noninvasive prenatal test result unconfirmed by invasive prenatal diagnosis.

Authors:  Jingmei Ma; David S Cram; Jianguang Zhang; Ling Shang; Huixia Yang; Hong Pan
Journal:  Mol Cytogenet       Date:  2015-06-26       Impact factor: 2.009

6.  Detection of structural mosaicism from targeted and whole-genome sequencing data.

Authors:  Daniel A King; Alejandro Sifrim; Tomas W Fitzgerald; Raheleh Rahbari; Emma Hobson; Tessa Homfray; Sahar Mansour; Sarju G Mehta; Mohammed Shehla; Susan E Tomkins; Pradeep C Vasudevan; Matthew E Hurles
Journal:  Genome Res       Date:  2017-08-30       Impact factor: 9.043

7.  Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families.

Authors:  Anne S Soehn; Tim W Rattay; Stefanie Beck-Wödl; Karin Schäferhoff; David Monk; Marion Döbler-Neumann; Konstanze Hörtnagel; Agatha Schlüter; Montserrat Ruiz; Aurora Pujol; Stephan Züchner; Olaf Riess; Rebecca Schüle; Peter Bauer; Ludger Schöls
Journal:  Neurology       Date:  2016-06-17       Impact factor: 9.910

8.  Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure.

Authors:  Thomas Eggermann
Journal:  Geburtshilfe Frauenheilkd       Date:  2021-07-13       Impact factor: 2.915

Review 9.  Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci.

Authors:  Thomas Eggermann; Guiomar Perez de Nanclares; Eamonn R Maher; I Karen Temple; Zeynep Tümer; David Monk; Deborah J G Mackay; Karen Grønskov; Andrea Riccio; Agnès Linglart; Irène Netchine
Journal:  Clin Epigenetics       Date:  2015-11-14       Impact factor: 6.551

10.  Causal variants screened by whole exome sequencing in a patient with maternal uniparental isodisomy of chromosome 10 and a complicated phenotype.

Authors:  Niu Li; Y U Ding; Tingting Yu; Juan Li; Yongnian Shen; Xiumin Wang; Qihua Fu; Yiping Shen; Xiaodong Huang; Jian Wang
Journal:  Exp Ther Med       Date:  2016-04-11       Impact factor: 2.447

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