Literature DB >> 29656286

Classification of Uniparental Isodisomy Patterns That Cause Autosomal Recessive Disorders: Proposed Mechanisms of Different Proportions and Parental Origin in Each Pattern.

Yo Niida, Mamoru Ozaki, Masaki Shimizu, Kazuyuki Ueno, Tomomi Tanaka.   

Abstract

Patients with autosomal recessive (AR) disorders are usually born to parents both of whom are heterozygous carriers of the disease. However, in some instances only one of the parents is a carrier and a mutation is segregated to the patient through uniparental isodisomy (UPiD). Recently, an increasing number of such case reports has been published, and it has become clear that there are several different UPiD patterns that cause AR disorders. In this article, we report 3 remarkable patients with different patterns of UPiD. We then review 85 cases collected in the literature. We realized that they can be classified into 3 patterns: UPiD of the whole chromosome, segmental UPiD with uniparental heterodisomy (UPhD), and segmental UPiD caused by post-zygotic mitotic recombination (MiRe). Whole chromosomal UPiD accounted for the majority of cases, with paternal origin accounting for approximately twice as many cases as maternal origin. Most cases of segmental UPiD with UPhD were of maternal origin, with a dominancy of nondisjunction in meiosis I, while segmental UPiD through MiRe is the smallest pattern with equal parental origin. These differences in proportion and parental origin in each pattern can be explained by considering nondisjunction during oogenesis as the starting point and UPiD as subsequent events.
© 2018 S. Karger AG, Basel.

Entities:  

Keywords:  Autosomal recessive disorders; Genetic counselling; Monosomy rescue; SNP array; Trisomy rescue; Uniparental isodisomy

Mesh:

Year:  2018        PMID: 29656286     DOI: 10.1159/000488572

Source DB:  PubMed          Journal:  Cytogenet Genome Res        ISSN: 1424-8581            Impact factor:   1.636


  9 in total

1.  De novo unbalanced translocations have a complex history/aetiology.

Authors:  Maria Clara Bonaglia; Nehir Edibe Kurtas; Edoardo Errichiello; Sara Bertuzzo; Silvana Beri; Mana M Mehrjouy; Aldesia Provenzano; Debora Vergani; Vanna Pecile; Francesca Novara; Paolo Reho; Marilena Carmela Di Giacomo; Giancarlo Discepoli; Roberto Giorda; Micheala A Aldred; Cíntia Barros Santos-Rebouças; Andressa Pereira Goncalves; Diane N Abuelo; Sabrina Giglio; Ivana Ricca; Fabrizia Franchi; Philippos Patsalis; Carolina Sismani; María Angeles Morí; Julián Nevado; Niels Tommerup; Orsetta Zuffardi
Journal:  Hum Genet       Date:  2018-10-01       Impact factor: 4.132

2.  Uniparental disomy in a population of 32,067 clinical exome trios.

Authors:  Julie Scuffins; Jennifer Keller-Ramey; Lindsay Dyer; Ganka Douglas; Rebecca Torene; Vladimir Gainullin; Jane Juusola; Jeanne Meck; Kyle Retterer
Journal:  Genet Med       Date:  2021-01-25       Impact factor: 8.822

3.  Uniparental isodisomy caused autosomal recessive diseases: NGS-based analysis allows the concurrent detection of homogenous variants and copy-neutral loss of heterozygosity.

Authors:  Bing Xiao; Lili Wang; Huili Liu; Yanjie Fan; Yan Xu; Yu Sun; Wenjuan Qiu
Journal:  Mol Genet Genomic Med       Date:  2019-08-27       Impact factor: 2.183

4.  Case Report: Partial Uniparental Disomy Unmasks a Novel Recessive Mutation in the LYST Gene in a Patient With a Severe Phenotype of Chédiak-Higashi Syndrome.

Authors:  Mireia Boluda-Navarro; Mariam Ibáñez; Alessandro Liquori; Clara Franco-Jarava; Mónica Martínez-Gallo; Héctor Rodríguez-Vega; Jaijo Teresa; Carmen Carreras; Esperanza Such; Ángel Zúñiga; Roger Colobran; José Vicente Cervera
Journal:  Front Immunol       Date:  2021-03-31       Impact factor: 7.561

Review 5.  The genetics of mitochondrial disease: dissecting mitochondrial pathology using multi-omic pipelines.

Authors:  Charlotte L Alston; Sarah L Stenton; Gavin Hudson; Holger Prokisch; Robert W Taylor
Journal:  J Pathol       Date:  2021-03-26       Impact factor: 9.883

6.  Heterogeneous genetic landscape of congenital neutropenia in Korean patients revealed by whole exome sequencing: genetic, phenotypic and histologic correlations.

Authors:  Dajeong Jeong; Sung-Min Kim; Byung Joo Min; Ju Han Kim; Young Seok Ju; Yong-Oon Ahn; Jiwon Yun; Young Eun Lee; Seok Ryun Kwon; Jae Hyeon Park; Jong Hyun Yoon; Dong Soon Lee
Journal:  Sci Rep       Date:  2022-05-07       Impact factor: 4.996

7.  Spectrum of germline AIRE mutations causing APS-1 and familial hypoparathyroidism.

Authors:  Treena Cranston; Hannah Boon; Mie K Olesen; Fiona J Ryan; Deborah Shears; Rosemary London; Hussam Rostom; Taha Elajnaf; Rajesh V Thakker; Fadil M Hannan
Journal:  Eur J Endocrinol       Date:  2022-05-24       Impact factor: 6.558

8.  Homozygosity for a Novel DOCK7 Variant Due to Segmental Uniparental Isodisomy of Chromosome 1 Associated with Early Infantile Epileptic Encephalopathy (EIEE) and Cortical Visual Impairment.

Authors:  Fatma Kivrak Pfiffner; Samuel Koller; Anika Ménétrey; Urs Graf; Luzy Bähr; Alessandro Maspoli; Annette Hackenberg; Raimund Kottke; Christina Gerth-Kahlert; Wolfgang Berger
Journal:  Int J Mol Sci       Date:  2022-07-02       Impact factor: 6.208

9.  LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy.

Authors:  Pere Soler-Palacín; Marina Garcia-Prat; Andrea Martín-Nalda; Clara Franco-Jarava; Jacques G Rivière; Alberto Plaja; Daniela Bezdan; Mattia Bosio; Mónica Martínez-Gallo; Stephan Ossowski; Roger Colobran
Journal:  Front Immunol       Date:  2018-10-16       Impact factor: 7.561

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.