TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly

Mutations in TBX22 are known causes of cleft palate with/without ankyloglossia. We identified a hemizygous missense c.452G>T (p.Arg151Leu) mutation in a Thai boy who had unilateral complete cleft lip and palate, agenesis of a maxillary second premolar, ankyloglossia, hypoplastic carpal bones, and...

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Main Authors: Kaewkhampa A., Jotikasthira D., Malaivijitnond S., Kantaputra P.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-84858612750&partnerID=40&md5=1661983d125cfafa8b1b2fbe988b7a93
http://cmuir.cmu.ac.th/handle/6653943832/1144
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Institution: Chiang Mai University
Language: English
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spelling th-cmuir.6653943832-11442014-08-29T09:17:48Z TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly Kaewkhampa A. Jotikasthira D. Malaivijitnond S. Kantaputra P. Mutations in TBX22 are known causes of cleft palate with/without ankyloglossia. We identified a hemizygous missense c.452G>T (p.Arg151Leu) mutation in a Thai boy who had unilateral complete cleft lip and palate, agenesis of a maxillary second premolar, ankyloglossia, hypoplastic carpal bones, and hypoplastic right thumb. Our study has demonstrated that TBX22 mutation is associated not only with cleft palate and ankyloglossia, but also cleft lip and palate and tooth agenesis. Phenotypic variability caused by a single nucleotide substitution is clearly demonstrated. 2014-08-29T09:17:48Z 2014-08-29T09:17:48Z 2012 Article 10556656 10.1597/10-208 CPJOE http://www.scopus.com/inward/record.url?eid=2-s2.0-84858612750&partnerID=40&md5=1661983d125cfafa8b1b2fbe988b7a93 http://cmuir.cmu.ac.th/handle/6653943832/1144 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Mutations in TBX22 are known causes of cleft palate with/without ankyloglossia. We identified a hemizygous missense c.452G>T (p.Arg151Leu) mutation in a Thai boy who had unilateral complete cleft lip and palate, agenesis of a maxillary second premolar, ankyloglossia, hypoplastic carpal bones, and hypoplastic right thumb. Our study has demonstrated that TBX22 mutation is associated not only with cleft palate and ankyloglossia, but also cleft lip and palate and tooth agenesis. Phenotypic variability caused by a single nucleotide substitution is clearly demonstrated.
format Article
author Kaewkhampa A.
Jotikasthira D.
Malaivijitnond S.
Kantaputra P.
spellingShingle Kaewkhampa A.
Jotikasthira D.
Malaivijitnond S.
Kantaputra P.
TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly
author_facet Kaewkhampa A.
Jotikasthira D.
Malaivijitnond S.
Kantaputra P.
author_sort Kaewkhampa A.
title TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly
title_short TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly
title_full TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly
title_fullStr TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly
title_full_unstemmed TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly
title_sort tbx22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-84858612750&partnerID=40&md5=1661983d125cfafa8b1b2fbe988b7a93
http://cmuir.cmu.ac.th/handle/6653943832/1144
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