Literature DB >> 26138576

Consanguinity as an Adjunct Diagnostic Tool.

Priyanka Srivastava1, Deepti Saxena1, Stephen Joshi1, Shubha R Phadke2.   

Abstract

History of consanguinity is important in monogenic disorders as it supports autosomal recessive mode of inheritance. This case report illustrates the use of homozygosity mapping using single nucleotide polymorphism (SNP) microarray data to identify the causative gene in a case with Warburg Micro syndrome (WARBM). This syndrome has non-specific features like microcephaly and cataract; etiological diagnosis based on clinical features is not possible. Four causative genes are known for WARBM syndrome. In such a situation of autosomal recessive disorders of heterogeneous etiologies, SNP microarray and homozygosity mapping is a useful and cost effective strategy.

Entities:  

Keywords:  Homozygosity mapping; India; Loss of heterozygosity; Micro syndrome; Mutation; RAB3GAP1

Mesh:

Substances:

Year:  2015        PMID: 26138576     DOI: 10.1007/s12098-015-1764-9

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  5 in total

1.  A homozygous RAB3GAP2 mutation causes Warburg Micro syndrome.

Authors:  Guntram Borck; Heidrun Wunram; Angela Steiert; Alexander E Volk; Friederike Körber; Sigrid Roters; Peter Herkenrath; Bernd Wollnik; Deborah J Morris-Rosendahl; Christian Kubisch
Journal:  Hum Genet       Date:  2010-10-22       Impact factor: 4.132

2.  Loss-of-function mutations in RAB18 cause Warburg micro syndrome.

Authors:  Danai Bem; Shin-Ichiro Yoshimura; Ricardo Nunes-Bastos; Frances C Bond; Frances F Bond; Manju A Kurian; Fatima Rahman; Mark T W Handley; Yavor Hadzhiev; Imran Masood; Ania A Straatman-Iwanowska; Andrew R Cullinane; Alisdair McNeill; Shanaz S Pasha; Gail A Kirby; Katharine Foster; Zubair Ahmed; Jenny E Morton; Denise Williams; John M Graham; William B Dobyns; Lydie Burglen; John R Ainsworth; Paul Gissen; Ferenc Müller; Eamonn R Maher; Francis A Barr; Irene A Aligianis
Journal:  Am J Hum Genet       Date:  2011-04-08       Impact factor: 11.025

3.  Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndrome.

Authors:  Irene A Aligianis; Colin A Johnson; Paul Gissen; Dongrong Chen; Daniel Hampshire; Katrin Hoffmann; Esther N Maina; Neil V Morgan; Louise Tee; Jenny Morton; John R Ainsworth; Denise Horn; Elisabeth Rosser; Trevor R P Cole; Irene Stolte-Dijkstra; Karen Fieggen; Jill Clayton-Smith; André Mégarbané; Julian P Shield; Ruth Newbury-Ecob; William B Dobyns; John M Graham; Klaus W Kjaer; Mette Warburg; Jacqueline Bond; Richard C Trembath; Laura W Harris; Yoshimi Takai; Stefan Mundlos; David Tannahill; C Geoffery Woods; Eamonn R Maher
Journal:  Nat Genet       Date:  2005-03       Impact factor: 38.330

4.  Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans.

Authors:  Ryan P Liegel; Mark T Handley; Adam Ronchetti; Stephen Brown; Lars Langemeyer; Andrea Linford; Bo Chang; Deborah J Morris-Rosendahl; Sarah Carpanini; Renata Posmyk; Verity Harthill; Eamonn Sheridan; Ghada M H Abdel-Salam; Paulien A Terhal; Francesca Faravelli; Patrizia Accorsi; Lucio Giordano; Lorenzo Pinelli; Britta Hartmann; Allison D Ebert; Francis A Barr; Irene A Aligianis; Duska J Sidjanin
Journal:  Am J Hum Genet       Date:  2013-11-14       Impact factor: 11.025

5.  A clinical evaluation tool for SNP arrays, especially for autosomal recessive conditions in offspring of consanguineous parents.

Authors:  Klaas J Wierenga; Zhijie Jiang; Amy C Yang; John J Mulvihill; Nicholas F Tsinoremas
Journal:  Genet Med       Date:  2012-10-25       Impact factor: 8.822

  5 in total
  1 in total

1.  Novel RAB3GAP1 Mutation in the First Tunisian Family With Warburg Micro Syndrome.

Authors:  Nesrine Kerkeni; Maher Kharrat; Faouzi Maazoul; Hela Boudabous; Ridha M'rad; Mediha Trabelsi
Journal:  J Clin Neurol       Date:  2022-02-14       Impact factor: 3.077

  1 in total

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