Mutations in FGFR3 gene associated with maxillary retrognathism

Context: Understanding the role of fibroblast growth factor receptor (FGFR) in the regulation of bone development and disease will ultimately lead to better prevention and treatment of related bone deformities and disorders. Aims: To evaluate the role of gene FGFR3 in individuals with retrognathic m...

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Bibliographic Details
Main Authors: Ravi M Subrahmanya (Author), Sreenivas V Prasad (Author), Rajendra B Prasad (Author), Subraya Mogra (Author), Veena Shetty (Author), Vamana Rao (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2019-01-01T00:00:00Z.
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001 doaj_8ed378a93bc0441cae7f96a82a7c051c
042 |a dc 
100 1 0 |a Ravi M Subrahmanya  |e author 
700 1 0 |a Sreenivas V Prasad  |e author 
700 1 0 |a Rajendra B Prasad  |e author 
700 1 0 |a Subraya Mogra  |e author 
700 1 0 |a Veena Shetty  |e author 
700 1 0 |a Vamana Rao  |e author 
245 0 0 |a Mutations in FGFR3 gene associated with maxillary retrognathism 
260 |b Wolters Kluwer Medknow Publications,   |c 2019-01-01T00:00:00Z. 
500 |a 0970-9290 
500 |a 1998-3603 
500 |a 10.4103/ijdr.IJDR_113_18 
520 |a Context: Understanding the role of fibroblast growth factor receptor (FGFR) in the regulation of bone development and disease will ultimately lead to better prevention and treatment of related bone deformities and disorders. Aims: To evaluate the role of gene FGFR3 in individuals with retrognathic maxilla by polymerase chain reaction (PCR) technique at molecular level and evaluate the significance of the same. Settings and Design: Hospital based fundamental research involving individuals having maxillary retrognathism. Methodology: A total of 62 individuals (30M and32F) who were willing to take part in the study were selected from cephalometric measurements of N I A and the length PNS to ANS. The institution based basic genetic research study involved collection of fresh blood samples, DNA extraction, PCR analysis, and amplification using the specifically designed forward and reverse primers for targeting the commonly occurring mutations in FGFR3 gene. Further the products were sequenced to evaluate the presence of any novel mutations. Results: The targeted single-nucleotide polymorphisms, at position 1138 in exon 10 of the FGFR3 gene were not identified in the analyzed blood samples. The detailed sequencing of full gene revealed the presence of 2 novel mutations, Exon 3: A213G and Exon 3: A223A/G in one individual. Conclusions: The present study indicated 2 novel mutations in gene FGFR3 in individual with maxillary retrognathism. The genetic-environmental interactions might have played a significant role in the expression of retrognathic maxilla. 
546 |a EN 
690 |a Gene FGFR3 
690 |a mutations 
690 |a retrognathic maxilla 
690 |a Dentistry 
690 |a RK1-715 
655 7 |a article  |2 local 
786 0 |n Indian Journal of Dental Research, Vol 30, Iss 2, Pp 185-190 (2019) 
787 0 |n http://www.ijdr.in/article.asp?issn=0970-9290;year=2019;volume=30;issue=2;spage=185;epage=190;aulast=Subrahmanya 
787 0 |n https://doaj.org/toc/0970-9290 
787 0 |n https://doaj.org/toc/1998-3603 
856 4 1 |u https://doaj.org/article/8ed378a93bc0441cae7f96a82a7c051c  |z Connect to this object online.