Article
Natural history and manifestations of the hypermobility type Ehlers-Danlos syndrome: a pilot study on 21 patients.
American journal of medical genetics. Part A - 1 Mar 2010
Castori Marco, Camerota Filippo, Celletti Claudia, Danese Chiara, Santilli Valter, Saraceni Vincenzo Maria, Grammatico Paola
Abstract excerpt
Hypermobility type Ehlers-Danlos syndrome (HT-EDS) is a relatively frequent, although commonly misdiagnosed variant of Ehlers-Danlos syndrome, mainly characterized by marked joint instability and mild cutaneous involvement. Chronic pain, asthenia, and gastrointestinal and pelvic dysfunction are characteristic additional manifestations. We report on 21 HT-EDS patients selected from a group of 40 subjects with...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
