SAGE open medicine · 2020
Whole exome sequencing identifies compound heterozygous variants of CR2 gene in monozygotic twin patients with common variable immunodeficiency.
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Mat Ripen Adiratna, Ghani Hamidah, Chear Chai Teng, Chiow Mei Yee, Syed Yahya Sharifah Nurul Husna, Kassim Asiah, Mohamad Saharuddin Bin
Аннотация
OBJECTIVES: A pair of female Malay monozygotic twins who presented with recurrent upper respiratory tract infections, hepatosplenomegaly, bronchiectasis and bicytopenia were recruited in this study. Both patients were suspected with primary immunodeficiency diseases. However, the definite diagnosis was not clear due to complex disease phenotypes. The objective of this study was to identify the causative gene mutation in these patients.
METHODS: Lymphocyte subset enumeration test and whole exome sequencing were performed.
RESULTS: We identified a compound heterozygous CR2 mutation (c.1916G>A and c.2012G>A) in both patients. These variants were then confirmed using Sanger sequencing.
CONCLUSION: Whole exome sequencing analysis of the monozygotic twins revealed compound heterozygous missense mutations in CR2.
METHODS: Lymphocyte subset enumeration test and whole exome sequencing were performed.
RESULTS: We identified a compound heterozygous CR2 mutation (c.1916G>A and c.2012G>A) in both patients. These variants were then confirmed using Sanger sequencing.
CONCLUSION: Whole exome sequencing analysis of the monozygotic twins revealed compound heterozygous missense mutations in CR2.