Autosomal recessive multiple epiphyseal dysplasia in a korean girl caused by novel compound heterozygous mutations in the DTDST (SLC26A2) gene

Tae Joon Cho, Ok Hwa Kim, Hye Ran Lee, Sung Jin Shin, Won Joon Yoo, Woong Yang Park, Sung Sup Park, Sung Im Cho, In Ho Choi

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)1105-1108
Number of pages4
JournalJournal of Korean Medical Science
Volume25
Issue number7
DOIs
StatePublished - Jul 2010
Externally publishedYes

Keywords

  • Diastrophic dysplasia sulfate transporter
  • Osteochondrodysplasias

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