Literature DB >> 27427187

Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencing.

R Del Orbe Barreto1, B Arrizabalaga1,2, A B De la Hoz1, Á García-Orad1,3, M I Tejada1,4, J C Garcia-Ruiz1,2, T Fidalgo5, C Bento5, L Manco6, M L Ribeiro5.   

Abstract

INTRODUCTION: Congenital haemolytic anaemia (CHA) refers to a group of genetically heterogeneous disorders, mainly caused by changes in genes encoding globin chains, cytoskeletal proteins and red cell enzymes, in which accurate diagnosis can be challenging with conventional techniques.
METHODS: To set-up a comprehensive assay for detecting mutations that could improve aetiological diagnosis, we designed a custom panel for sequencing coding regions from 40 genes known to be involved in the pathogenesis of CHA, using the Ion Torrent™ (Thermo Fisher Scientific, S.L. Waltham, MA, USA) Personal Genome Machine (PGM) Sequencer. A control group of 16 samples with previously known mutations and a test group of 10 patients with unknown mutations were included for assay validation and application, respectively.
RESULTS: In the test group, we identified pathogenic mutations in all cases: four patients had novel mutations in genes related to membrane defects (SPTB, ANK1, SLC4A1 and EPB41), four were homozygous or compound heterozygous for mutations in genes related to enzyme deficiencies (GPI, TPI1 and GSS), one had a mutation in the HBB gene and another presented a homozygous mutation in the ADAMTS13 gene.
CONCLUSIONS: Ion PGM sequencing with our custom panel is a highly efficient way to detect mutations causing haemolytic anaemia, including new variations. It is a high-throughput detection method that is ready for application in clinical laboratories.
© 2016 John Wiley & Sons Ltd.

Entities:  

Keywords:  Congenital anaemia; haemolysis; molecular diagnosis; mutations; next-generation sequencing

Mesh:

Year:  2016        PMID: 27427187     DOI: 10.1111/ijlh.12551

Source DB:  PubMed          Journal:  Int J Lab Hematol        ISSN: 1751-5521            Impact factor:   2.877


  12 in total

1.  Study of pathophysiology and molecular characterization of congenital anemia in India using targeted next-generation sequencing approach.

Authors:  Prabhakar S Kedar; Hideo Harigae; Etsuro Ito; Hideki Muramatsu; Seiji Kojima; Yusuke Okuno; Tohru Fujiwara; Rashmi Dongerdiye; Prashant P Warang; Manisha R Madkaikar
Journal:  Int J Hematol       Date:  2019-08-10       Impact factor: 2.490

2.  Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency.

Authors:  Paola Bianchi; Elisa Fermo; Bertil Glader; Hitoshi Kanno; Archana Agarwal; Wilma Barcellini; Stefan Eber; James D Hoyer; David J Kuter; Tabita Magalhães Maia; Maria Del Mar Mañu-Pereira; Theodosia A Kalfa; Serge Pissard; José-Carlos Segovia; Eduard van Beers; Patrick G Gallagher; David C Rees; Richard van Wijk
Journal:  Am J Hematol       Date:  2018-11-28       Impact factor: 10.047

Review 3.  Diagnostic approaches for inherited hemolytic anemia in the genetic era.

Authors:  Yonggoo Kim; Joonhong Park; Myungshin Kim
Journal:  Blood Res       Date:  2017-06-22

4.  Exome sequencing for diagnosis of congenital hemolytic anemia.

Authors:  Lamisse Mansour-Hendili; Abdelrazak Aissat; Bouchra Badaoui; Mehdi Sakka; Christine Gameiro; Valérie Ortonne; Orianne Wagner-Ballon; Serge Pissard; Véronique Picard; Khaldoun Ghazal; Michel Bahuau; Corinne Guitton; Ziad Mansour; Mylène Duplan; Arnaud Petit; Nathalie Costedoat-Chalumeau; Marc Michel; Pablo Bartolucci; Stéphane Moutereau; Benoît Funalot; Frédéric Galactéros
Journal:  Orphanet J Rare Dis       Date:  2020-07-08       Impact factor: 4.123

5.  A de novo ANK1 mutation associated to hereditary spherocytosis: a case report.

Authors:  Ti-Long Huang; Bao-Hua Sang; Qing-Ling Lei; Chun-Yan Song; Yun-Bi Lin; Yu Lv; Chun-Hui Yang; Na Li; Yue-Huang Yang; Xian-Wen Zhang; Xin Tian
Journal:  BMC Pediatr       Date:  2019-02-18       Impact factor: 2.125

Review 6.  Genetics and Genomics Approaches for Diagnosis and Research Into Hereditary Anemias.

Authors:  Roberta Russo; Roberta Marra; Barbara Eleni Rosato; Achille Iolascon; Immacolata Andolfo
Journal:  Front Physiol       Date:  2020-12-22       Impact factor: 4.566

7.  Targeted Next Generation Sequencing and Diagnosis of Congenital Hemolytic Anemias: A Three Years Experience Monocentric Study.

Authors:  Elisa Fermo; Cristina Vercellati; Anna Paola Marcello; Ebru Yilmaz Keskin; Silverio Perrotta; Anna Zaninoni; Valentina Brancaleoni; Alberto Zanella; Juri A Giannotta; Wilma Barcellini; Paola Bianchi
Journal:  Front Physiol       Date:  2021-05-21       Impact factor: 4.566

8.  An ANK1 IVS3-2A>C mutation causes exon 4 skipping in two patients from a Chinese family with hereditary spherocytosis.

Authors:  Xiong Wang; Liyan Mao; Na Shen; Jing Peng; Yaowu Zhu; Qun Hu; Yanjun Lu
Journal:  Oncotarget       Date:  2017-12-05

Review 9.  Molecular heterogeneity of pyruvate kinase deficiency.

Authors:  Paola Bianchi; Elisa Fermo
Journal:  Haematologica       Date:  2020-09-01       Impact factor: 9.941

10.  Combined study of ADAMTS13 and complement genes in the diagnosis of thrombotic microangiopathies using next-generation sequencing.

Authors:  Teresa Fidalgo; Patrícia Martinho; Catarina S Pinto; Ana C Oliveira; Ramon Salvado; Nina Borràs; Margarida Coucelo; Licínio Manco; Tabita Maia; M João Mendes; Rafael Del Orbe Barreto; Irene Corrales; Francisco Vidal; M Letícia Ribeiro
Journal:  Res Pract Thromb Haemost       Date:  2017-06-23
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