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Tenascin-X deficiency and Ehlers-Danlos syndrome: a case report and review of the literature M. O'Connell et al. Tenascin-X deficiency and Ehlers-Danlos syndrome.

Authors :
O'Connell, M.
Burrows, N. P.
Van Vlijmen-Willems, M. J. J.
Clark, S. M.
Schalkwijk, J.
Source :
British Journal of Dermatology. Dec2010, Vol. 163 Issue 6, p1340-1345. 6p.
Publication Year :
2010

Abstract

Tenascin-X is a large extracellular matrix glycoprotein that is widely distributed within connective tissues and is associated with an autosomal recessive type of Ehlers-Danlos syndrome (EDS). Tenascin-X represents the first EDS susceptibility gene that does not code for a fibrillar collagen or collagen-processing enzyme. We describe a paediatric case of tenascin-X deficiency and review the literature. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00070963
Volume :
163
Issue :
6
Database :
Academic Search Index
Journal :
British Journal of Dermatology
Publication Type :
Academic Journal
Accession number :
55255660
Full Text :
https://doi.org/10.1111/j.1365-2133.2010.09949.x