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Autosomal Recessive Multiple Epiphyseal Dysplasia in a Korean Girl Caused by Novel Compound Heterozygous Mutations in the DTDST (SLC26A2) Gene

Multiple epiphyseal dysplasia is caused by heterogenous genotypes involving more than six genes. Recessive mutations in the DTDST gene cause a phenotype of recessive multiple epiphyseal dysplasia (rMED). The authors report a 9-yr old Korean girl with the rMED phenotype having novel compound heterozy...

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Autores principales: Cho, Tae-Joon, Kim, Ok-Hwa, Lee, Hye-Ran, Shin, Sung Jin, Yoo, Won Joon, Park, Woong Yang, Park, Sung Sup, Cho, Sung Im, Choi, In Ho
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890895/
https://www.ncbi.nlm.nih.gov/pubmed/20592910
http://dx.doi.org/10.3346/jkms.2010.25.7.1105
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author Cho, Tae-Joon
Kim, Ok-Hwa
Lee, Hye-Ran
Shin, Sung Jin
Yoo, Won Joon
Park, Woong Yang
Park, Sung Sup
Cho, Sung Im
Choi, In Ho
author_facet Cho, Tae-Joon
Kim, Ok-Hwa
Lee, Hye-Ran
Shin, Sung Jin
Yoo, Won Joon
Park, Woong Yang
Park, Sung Sup
Cho, Sung Im
Choi, In Ho
author_sort Cho, Tae-Joon
collection PubMed
description Multiple epiphyseal dysplasia is caused by heterogenous genotypes involving more than six genes. Recessive mutations in the DTDST gene cause a phenotype of recessive multiple epiphyseal dysplasia (rMED). The authors report a 9-yr old Korean girl with the rMED phenotype having novel compound heterozygous mutations in the DTDST gene, which were inherited from both parents. This is the first Korean rMED case attributed to DTDST mutations, and expands the spectrum of diseases caused by DTDST mutations.
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spelling pubmed-28908952010-07-01 Autosomal Recessive Multiple Epiphyseal Dysplasia in a Korean Girl Caused by Novel Compound Heterozygous Mutations in the DTDST (SLC26A2) Gene Cho, Tae-Joon Kim, Ok-Hwa Lee, Hye-Ran Shin, Sung Jin Yoo, Won Joon Park, Woong Yang Park, Sung Sup Cho, Sung Im Choi, In Ho J Korean Med Sci Case Report Multiple epiphyseal dysplasia is caused by heterogenous genotypes involving more than six genes. Recessive mutations in the DTDST gene cause a phenotype of recessive multiple epiphyseal dysplasia (rMED). The authors report a 9-yr old Korean girl with the rMED phenotype having novel compound heterozygous mutations in the DTDST gene, which were inherited from both parents. This is the first Korean rMED case attributed to DTDST mutations, and expands the spectrum of diseases caused by DTDST mutations. The Korean Academy of Medical Sciences 2010-07 2010-06-16 /pmc/articles/PMC2890895/ /pubmed/20592910 http://dx.doi.org/10.3346/jkms.2010.25.7.1105 Text en © 2010 The Korean Academy of Medical Sciences. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Cho, Tae-Joon
Kim, Ok-Hwa
Lee, Hye-Ran
Shin, Sung Jin
Yoo, Won Joon
Park, Woong Yang
Park, Sung Sup
Cho, Sung Im
Choi, In Ho
Autosomal Recessive Multiple Epiphyseal Dysplasia in a Korean Girl Caused by Novel Compound Heterozygous Mutations in the DTDST (SLC26A2) Gene
title Autosomal Recessive Multiple Epiphyseal Dysplasia in a Korean Girl Caused by Novel Compound Heterozygous Mutations in the DTDST (SLC26A2) Gene
title_full Autosomal Recessive Multiple Epiphyseal Dysplasia in a Korean Girl Caused by Novel Compound Heterozygous Mutations in the DTDST (SLC26A2) Gene
title_fullStr Autosomal Recessive Multiple Epiphyseal Dysplasia in a Korean Girl Caused by Novel Compound Heterozygous Mutations in the DTDST (SLC26A2) Gene
title_full_unstemmed Autosomal Recessive Multiple Epiphyseal Dysplasia in a Korean Girl Caused by Novel Compound Heterozygous Mutations in the DTDST (SLC26A2) Gene
title_short Autosomal Recessive Multiple Epiphyseal Dysplasia in a Korean Girl Caused by Novel Compound Heterozygous Mutations in the DTDST (SLC26A2) Gene
title_sort autosomal recessive multiple epiphyseal dysplasia in a korean girl caused by novel compound heterozygous mutations in the dtdst (slc26a2) gene
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890895/
https://www.ncbi.nlm.nih.gov/pubmed/20592910
http://dx.doi.org/10.3346/jkms.2010.25.7.1105
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