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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...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Korean Academy of Medical Sciences
2010
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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. |
format | Text |
id | pubmed-2890895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
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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