Literature DB >> 22339077

Rapid detection of G1138A and G1138C mutations of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis.

Xiang He1, Feng Xie, Zhao-rui Ren.   

Abstract

Achondroplasia (ACH) is a genetic disorder with autosomal dominant inheritance and is the cause of one of the most common forms of short limb dwarfism in humans. Mutations of special sites in the fibroblast growth factor receptor-3 gene (FGFR3) are reported as a cause of ACH, and almost 98% of cases are caused by mutations in nucleotide 1138 (Gly380Arg), with 97% involving a c.1138G>A mutation and 1% involving a c.1138G>C mutation. Therefore, the development of a simple, reliable, and rapid approach for molecular detection of nucleotide 1138 mutations is of great significance for prevention and early diagnosis of ACH. High-resolution melting (HRM) is a new, rapid, and inexpensive molecular detection method that has been generally applied to mutation scanning. In this study, 12 cases of ACH, including 10 sporadic cases and 2 cases in a pedigree, were detected simultaneously using HRM analysis and restriction fragment length polymorphism-polymerase chain reaction (RFLP-PCR). Eleven cases were identified as carrying the c.1138 G>A heterozygous mutation, and one case was identified as carrying the c.1138 G>C heterozygous mutation. Compared with RFLP-PCR, HRM analysis provided a more rapid, simpler, and less expensive approach for detecting the most common FGFR3 mutations carried by patients with ACH.

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Year:  2012        PMID: 22339077     DOI: 10.1089/gtmb.2011.0113

Source DB:  PubMed          Journal:  Genet Test Mol Biomarkers        ISSN: 1945-0257


  7 in total

Review 1.  Advances in research on and diagnosis and treatment of achondroplasia in China.

Authors:  Yao Wang; Zeying Liu; Zhenxing Liu; Heng Zhao; Xiaoyan Zhou; Yazhou Cui; Jinxiang Han
Journal:  Intractable Rare Dis Res       Date:  2013-05

2.  Novel and Recurrent Mutations in the FGFR3 Gene and Double Heterozygosity Cases in a Cohort of Brazilian Patients with Skeletal Dysplasia.

Authors:  Maria E S Gomes; Thatiane Y Kanazawa; Fernanda R Riba; Natálya G Pereira; Maria C C Zuma; Natana C Rabelo; Maria T Sanseverino; Dafne D G Horovitz; Juan C Llerena; Denise P Cavalcanti; Sayonara Gonzalez
Journal:  Mol Syndromol       Date:  2018-02-02

3.  Analysis of the clinical and molecular characteristics of a child with achondroplasia: A case report.

Authors:  Jingfang Liu; Xulei Tang; Jianguo Cheng; Liting Wang; Xiaomei Yang; Yan Wang
Journal:  Exp Ther Med       Date:  2015-03-02       Impact factor: 2.447

4.  Diagnostic, treatment and outcome possibilities in achondroplasia.

Authors:  Simona Bucerzan; Camelia Alkhzouz; Mirela Crisan; Diana Miclea; Carmen Asavoaie; Roxana Ilies; Paula Grigorescu-Sido
Journal:  Med Pharm Rep       Date:  2021-08-10

5.  FGFR3 gene mutation plus GRB10 gene duplication in a patient with achondroplasia plus growth delay with prenatal onset.

Authors:  Haiming Yuan; Linhuan Huang; Xizi Hu; Qian Li; Xiaofang Sun; Yingjun Xie; Shu Kong; Xiaoman Wang
Journal:  Orphanet J Rare Dis       Date:  2016-07-02       Impact factor: 4.123

6.  Identification and in silico characterization of p.G380R substitution in FGFR3, associated with achondroplasia in a non-consanguineous Pakistani family.

Authors:  Muhammad Ajmal; Asif Mir; Muhammad Shoaib; Salman Akbar Malik; Muhammad Nasir
Journal:  Diagn Pathol       Date:  2017-07-05       Impact factor: 2.644

7.  Molecular Confirmation of G1138A Mutation in FGFR gene in Achondroplasia.

Authors:  Shyam Bahadur Khanal; Mitesh Shrestha; Hemanta Kumari Chaudhary; Smita Shrestha; Rohit Kumar Pokharel
Journal:  JNMA J Nepal Med Assoc       Date:  2018 Mar-Apr       Impact factor: 0.406

  7 in total

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