International Journal of Molecular and Cellular Medicine (IJMCM)
Cellular and Molecular Biology Research Center, Babol University of Medical Sciences
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Volume 12, Issue 1 (Int J Mol Cell Med 2023)
Int J Mol Cell Med 2023, 12(1): 40-50 |
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Sardarpour N, Bagherian H, Zafarghandi motlagh F, Shirzadeh T, Asnavandi S, Younesikhah S, et al . Mutational Analysis and Genotype Investigation of Less Known Gaucher Mutations through Haplotype Analysis in Iranian Gaucher Patients. Int J Mol Cell Med 2023; 12 (1) :40-50
URL: http://ijmcmed.org/article-1-2035-en.html
URL: http://ijmcmed.org/article-1-2035-en.html
Negar Sardarpour1 
, Hamideh Bagherian2 , Fatemeh Zafarghandi motlagh2 , Tina Shirzadeh2 , Sadaf Asnavandi2 , Shahrzad Younesikhah2 , Shadab Salehpour3 , Aria Setoodeh4 , Mohammad Reza Alaei3 , Sirous Zeinali 5
, Hamideh Bagherian2 , Fatemeh Zafarghandi motlagh2 , Tina Shirzadeh2 , Sadaf Asnavandi2 , Shahrzad Younesikhah2 , Shadab Salehpour3 , Aria Setoodeh4 , Mohammad Reza Alaei3 , Sirous Zeinali 5
1- Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran.
2- Medical Genetics Lab of Dr. Zeinali, Kawsar Human Genetics Research Center, No. 41 Majlesi St., Vali Asr St, Tehran, Iran.
3- Department of Pediatric Endocrinology and Metabolism, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
4- Growth and Development Research Center, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
5- ,zeinali@gmail.com
2- Medical Genetics Lab of Dr. Zeinali, Kawsar Human Genetics Research Center, No. 41 Majlesi St., Vali Asr St, Tehran, Iran.
3- Department of Pediatric Endocrinology and Metabolism, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
4- Growth and Development Research Center, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
5- ,
Abstract: (1003 Views)
Gaucher's disease (GD) is the most frequent lysosomal storage disorder resulting from a deficiency of the enzyme glucocerebrosidase (GBA) which causes the accumulation of glucocerebroside. More than 500 mutations have been reported on the GBA gene so far. In this study, we aimed to investigate more on the genotype of less known mutations through haplotype analysis to explain their disease-causing inheritance. Eight patients and three carriers from nine different families were enrolled in the study. DNA sequencing of all GBA gene’s exons was performed and pathogenicity of the mutations was investigated. Using GBA gene-linked STR markers, allele segregations were determined in some families. A total of six different mutations were determined. Five and three patients were identified to carry mutations in homozygous and compound heterozygote patterns respectively, three participants also were identified as carriers. The most prevalent mutations were c.1448 T>C and RecNcil, however, three less common mutations were identified (i.e., c.1223 C>T, c.1315 A>G, and c.1214 G>C). In conclusion, we evaluated six different mutations in Iranian patients and elucidated the inheritance of the three less-known mutations by linkage analysis.
Keywords: Gaucher disease, beta-glucocerebrosidase, lysosomal storage disorder, haplotype analysis, Iran
Type of Study: Original Article |
Subject:
Genetics & Disease
Received: 2022/11/11 | Accepted: 2023/08/29 | Published: 2023/09/19
Received: 2022/11/11 | Accepted: 2023/08/29 | Published: 2023/09/19
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