Ehlers-Danlos Syndrome, Hypermobility Type, Is Linked to Chromosome 8p22-8p21.1 in an Extended Belgian Family

Joint hypermobility is a common, mostly benign, finding in the general population. In a subset of individuals, however, it causes a range of clinical problems, mainly affecting the musculoskeletal system. Joint hypermobility often appears as a familial trait and is shared by several heritable connective tissue disorders, including the hypermobility subtype of the Ehlers-Danlos syndrome (EDS-HT) or benign joint hypermobility syndrome (BJHS). These hereditary conditions provide unique models for the study of the genetic basis of joint hypermobility. Nevertheless, these studies are largely hamper... Mehr ...

Verfasser: Delfien Syx
Sofie Symoens
Wouter Steyaert
Anne De Paepe
Paul J. Coucke
Fransiska Malfait
Dokumenttyp: Artikel
Erscheinungsdatum: 2015
Reihe/Periodikum: Disease Markers, Vol 2015 (2015)
Verlag/Hrsg.: Hindawi Limited
Schlagwörter: Medicine (General) / R5-920
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26524094
Datenquelle: BASE; Originalkatalog
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Link(s) : https://doi.org/10.1155/2015/828970