Published in: 12th Congress of Iranian Genetics Society
COI code: CIGS13_0285
Paper Language: English
How to Download This Paper
For Downloading the Fulltext of CIVILICA papers please visit the orginal Persian Section of website.
Authors Identification of a new gene for an Ehlers-Danlos syndrome-like connective tissue disorder in 5 Iranian patientsAriana Kariminejad - Kariminejad-Najmabadi Pathology and Genetics Center, Tehran Iran
Fransiska Malfait - Center for Medical Genetics, Ghent University Hospital, Belgium
Bita Bozorgmehr - Kariminejad-Najmabadi Pathology and Genetics Center, Tehran Iran
Tim Van Damme - Center for Medical Genetics, Ghent University Hospital, Belgium
Abstract:Galactosyltransferse II (β3GALT6) encoded by B3GALT6 is a key enzyme in the synthetic pathway of proteoglycans.Proteoglycans are important components of cell plasma membranes and extracellular matrices of connective tissue. By homozygosity mapping and candidate gene sequence analysis we were able to identify mutations in B3GALT6 in three independent Iranian families. The patients presented with a severe connective tissue disorder characterized by skin fragility,delayed wound healing, severe joint hyperlaxity and contractures, muscle hypotonia, intellectual disability, and aspondyloepiphyseal dysplasia with bone fragility and severe kyphoscoliosis. The phenotype was unique but had overlaps with several recessive Ehlers-Danlos variants and spondyloepiphyseal dysplasia with joint laxity. Affected individual’s fibroblasts exhibited a large decrease in ability to prime glycosaminoglycan synthesis together withimpaired glycanation of the small chondroitin/dermatan sulfate proteoglycan decorin, confirming β3GalT6 loss of function.Dermal electron microscopy disclosed abnormalities in collagen fibril organization, in line with the important regulatoryrole of decorin in this process. Our study emphasizes a crucial role for β3GalT6 in multiple developmental processes and shows that mutations in B3GALT6 can cause a multi-system disorder. In this study we identified a new gene with a unique connective tissue phenotype
COI code: CIGS13_0285
how to cite to this paper:If you want to refer to this article in your research, you can easily use the following in the resources and references section:
Kariminejad, Ariana; Fransiska Malfait; Bita Bozorgmehr & Tim Van Damme, 2014, Identification of a new gene for an Ehlers-Danlos syndrome-like connective tissue disorder in 5 Iranian patients, 12th Congress of Iranian Genetics Society, تهران, انجمن ژنتيك ايران, https://www.civilica.com/Paper-CIGS13-CIGS13_0285.htmlInside the text, wherever referred to or an achievement of this article is mentioned, after mentioning the article, inside the parental, the following specifications are written.
First Time: (Kariminejad, Ariana; Fransiska Malfait; Bita Bozorgmehr & Tim Van Damme, 2014)
Second and more: (Kariminejad; Malfait; Bozorgmehr & Van Damme, 2014)
For a complete overview of how to citation please review the following CIVILICA Guide (Citation)
Research Info Management
Export Citation info of this paper to research management softwares
New Related Papers
- Composition, distribution and economic importance of insect pests of prioritized aromatic plants in some growing of Ethiopia
- Quantitative genetic analysis of Dromedary camel (Camelus dromedaris) under pastoral management in central desert of Iran
- Bimolecular identification of M.ovinpeumoniae from nasal swab samples of sheep from various districts of Balochistan, Pakistan
- Salt and water stress of ACCase herbicides resistant and susceptible populations of rigid ryegrass (Lolium rigidum)
- A Monte Carlo study on Photoneutron Spectrum around Elekta SL75/25 18 MV linear accelerator
The Above articles are recently indexed in the related subjects
Iran Scientific Advertisment Netword
Share this paper
WHAT IS COI?
COI is a national code dedicated to all Iranian Conference and Journal Papers. the COI of each paper can be verified online.