X-Linked Spondyloepiphyseal Dysplasia Tarda: Identification of a TRAPPC2 Mutation in a Korean Pedigree.
10.3343/alm.2012.32.3.234
- Author:
Hyejin RYU
1
;
Joonhong PARK
;
Hyojin CHAE
;
Myungshin KIM
;
Yonggoo KIM
;
In Young OK
Author Information
1. Department of Laboratory Medicine, The Catholic University of Korea College of Medicine, Seoul, Korea. chez@catholic.ac.kr
- Publication Type:Case Reports
- Keywords:
Spondyloepiphyseal dysplasia;
X-linked spondyloepiphyseal dysplasia tarda;
TRAPPC2;
SEDL
- MeSH:
Adolescent;
Asian Continental Ancestry Group/*genetics;
DNA Mutational Analysis;
Exons;
Genetic Diseases, X-Linked/*genetics;
Humans;
Male;
Membrane Transport Proteins/*genetics;
Osteochondrodysplasias/*genetics/radiography;
Pedigree;
Republic of Korea;
Transcription Factors/*genetics
- From:Annals of Laboratory Medicine
2012;32(3):234-237
- CountryRepublic of Korea
- Language:English
-
Abstract:
Spondyloepiphyseal dysplasia (SED) comprises a heterogeneous group of skeletal dysplasias that primarily affect the epiphyses and vertebral bodies. Patients affected by SED usually exhibit short stature and experience early development of degenerative osteoarthritis. SED is subdivided into congenita and tarda forms according to the age at onset and clinical severity, and further subdivided into genetically different forms according to the mode of inheritance and the gene involved. We report a 14-yr-old Korean male who presented with a disproportionately short stature and a short trunk. A pedigree analysis of 3 generations with 6 affected persons revealed an X-linked recessive mode of inheritance. Mutation analysis of the TRAPPC2 (previously called SEDL) gene, the only gene associated with X-linked spondyloepiphyseal dysplasia tarda (X-linked SEDT; MIM 313400), was performed, and a splice-donor site mutation in intron 3 of the TRAPPC2 gene (c.93+5G>A) was identified in the proband and in his unaffected mother (a heterozygote). This mutation is one of the 2 most frequent mutations reported in the medical literature, and is known to result in exon 3 skipping. This is the first report of a genetically confirmed X-linked SEDT case in Korea and highlights the importance of recognizing the mode of inheritance in the diagnosis of X-linked SEDT.
