Mutation status of skeletal muscle contractile genes (tnnt3 and tpm2) among malay clubfoot patients: determination using pcr-dna sequencing analysis

Introduction Clubfoot or congenital talipes equinovarus (CTEV) is one of the most common congenital musculoskeletal anomalies and the incidence of 1 in 1000 births. Idiopathic and non-idiopathic clubfeet demonstrate calf muscle hypoplasia at birth which remains small even after corrective treatme...

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Main Author: Ariff, Mohamad Faris Md
Format: Thesis
Language:English
Published: 2022
Subjects:
Online Access:http://eprints.usm.my/62332/
http://eprints.usm.my/62332/1/Mohamad%20Faris%20Md%20Ariff-E.pdf
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author Ariff, Mohamad Faris Md
author_facet Ariff, Mohamad Faris Md
author_sort Ariff, Mohamad Faris Md
building USM Institutional Repository
collection Online Access
description Introduction Clubfoot or congenital talipes equinovarus (CTEV) is one of the most common congenital musculoskeletal anomalies and the incidence of 1 in 1000 births. Idiopathic and non-idiopathic clubfeet demonstrate calf muscle hypoplasia at birth which remains small even after corrective treatment of the clubfoot. We conducted this study to look for any skeletal gene mutations in idiopathic CTEV, as it is well described in non-idiopathic CTEV. Methodology This study was carried out in 33 idiopathic CTEV children that get their treatment in Hospital Universiti Sains Malaysia. Buccal swab was obtained from the child and the sample was sent to Human Genome Centre, Universiti Sains Malaysia (USM). DNA was extracted and purity was quantified. PCR was conducted in optimum condition and followed by agarose gel electrophoresis. DNA sequencing done and any mutations were observed and recorded. The results for DNA sequencing was analyzed statistically. Result In our study, no mutations detected in all the study participants for TPM2: c.308A>G and TNNT3: c.187C>A. Therefore, the association between the TPM2: c.308A>G and TNNT3: c.187C>A gene mutations and the clubfoot severity in Malay patients with idiopathic clubfoot was undetermined. No statistical analysis was conducted since the outcome of the dependent variable (TPM2: c.308A>G and TNNT3: c.187C>A mutations) was constant (no mutation). Conclusion No mutation was found in TPM2 and TNNT3 gene, hence the association with the clubfoot severity is undetermined. However, we cannot totally exclude the skeletal muscle genes as here are few more genes that are responsible for development and function of skeletal muscle.
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institution_category Local University
language English
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spelling usm-623322025-06-01T07:22:13Z http://eprints.usm.my/62332/ Mutation status of skeletal muscle contractile genes (tnnt3 and tpm2) among malay clubfoot patients: determination using pcr-dna sequencing analysis Ariff, Mohamad Faris Md RA440-440.87 Study and teaching. Research Introduction Clubfoot or congenital talipes equinovarus (CTEV) is one of the most common congenital musculoskeletal anomalies and the incidence of 1 in 1000 births. Idiopathic and non-idiopathic clubfeet demonstrate calf muscle hypoplasia at birth which remains small even after corrective treatment of the clubfoot. We conducted this study to look for any skeletal gene mutations in idiopathic CTEV, as it is well described in non-idiopathic CTEV. Methodology This study was carried out in 33 idiopathic CTEV children that get their treatment in Hospital Universiti Sains Malaysia. Buccal swab was obtained from the child and the sample was sent to Human Genome Centre, Universiti Sains Malaysia (USM). DNA was extracted and purity was quantified. PCR was conducted in optimum condition and followed by agarose gel electrophoresis. DNA sequencing done and any mutations were observed and recorded. The results for DNA sequencing was analyzed statistically. Result In our study, no mutations detected in all the study participants for TPM2: c.308A>G and TNNT3: c.187C>A. Therefore, the association between the TPM2: c.308A>G and TNNT3: c.187C>A gene mutations and the clubfoot severity in Malay patients with idiopathic clubfoot was undetermined. No statistical analysis was conducted since the outcome of the dependent variable (TPM2: c.308A>G and TNNT3: c.187C>A mutations) was constant (no mutation). Conclusion No mutation was found in TPM2 and TNNT3 gene, hence the association with the clubfoot severity is undetermined. However, we cannot totally exclude the skeletal muscle genes as here are few more genes that are responsible for development and function of skeletal muscle. 2022 Thesis NonPeerReviewed application/pdf en http://eprints.usm.my/62332/1/Mohamad%20Faris%20Md%20Ariff-E.pdf Ariff, Mohamad Faris Md (2022) Mutation status of skeletal muscle contractile genes (tnnt3 and tpm2) among malay clubfoot patients: determination using pcr-dna sequencing analysis. Masters thesis, Universiti Sains Malaysia.
spellingShingle RA440-440.87 Study and teaching. Research
Ariff, Mohamad Faris Md
Mutation status of skeletal muscle contractile genes (tnnt3 and tpm2) among malay clubfoot patients: determination using pcr-dna sequencing analysis
title Mutation status of skeletal muscle contractile genes (tnnt3 and tpm2) among malay clubfoot patients: determination using pcr-dna sequencing analysis
title_full Mutation status of skeletal muscle contractile genes (tnnt3 and tpm2) among malay clubfoot patients: determination using pcr-dna sequencing analysis
title_fullStr Mutation status of skeletal muscle contractile genes (tnnt3 and tpm2) among malay clubfoot patients: determination using pcr-dna sequencing analysis
title_full_unstemmed Mutation status of skeletal muscle contractile genes (tnnt3 and tpm2) among malay clubfoot patients: determination using pcr-dna sequencing analysis
title_short Mutation status of skeletal muscle contractile genes (tnnt3 and tpm2) among malay clubfoot patients: determination using pcr-dna sequencing analysis
title_sort mutation status of skeletal muscle contractile genes (tnnt3 and tpm2) among malay clubfoot patients: determination using pcr-dna sequencing analysis
topic RA440-440.87 Study and teaching. Research
url http://eprints.usm.my/62332/
http://eprints.usm.my/62332/1/Mohamad%20Faris%20Md%20Ariff-E.pdf