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Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type
Genetics in Medicine, 2010 Classic Ehlers-Danlos syndrome is a heritable connective tissue disorder characterized by skin hyperextensibility, fragile and soft skin, delayed wound healing with formation of atrophic scars, easy bruising, and generalized joint hypermobility.
Anne De Paëpe +2 more
exaly +2 more sources
Pregnancy outcome in joint hypermobility syndrome and Ehlers–Danlos syndrome
Acta Obstetricia Et Gynecologica Scandinavica, 2017 IntroductionAn increased risk of preterm birth in women with joint hypermobility syndrome or Ehlers-Danlos syndrome is suspected. Material and methodsIn this nationwide cohort study from 1997 through 2011, women with either joint hypermobility syndrome ...
Kari Johansson +2 more
exaly +2 more sources
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BMJ, 2019
### What you need to know Awareness of the Ehlers-Danlos syndromes (EDS) in the UK has risen over the past decade, in part due to high profile of EDS patient organisations and the EDS National Diagnostic Service commissioned in 2009. Significant advances in genetic testing have culminated in the publication of a new international classification in ...
Neeti, Ghali +2 more
openaire +2 more sources
### What you need to know Awareness of the Ehlers-Danlos syndromes (EDS) in the UK has risen over the past decade, in part due to high profile of EDS patient organisations and the EDS National Diagnostic Service commissioned in 2009. Significant advances in genetic testing have culminated in the publication of a new international classification in ...
Neeti, Ghali +2 more
openaire +2 more sources
Southern Medical Journal, 1981
We have described a patient with type 4 Ehlers-Danlos syndrome who died of a ruptured pulmonary artery. Of the six subtypes of Ehlers-Danlos syndrome, which can usually be clinically differentiated, only types 1 and 4 appear to be associated with a substantial risk of arterial rupture.
W, Pearl, M, Spicer
openaire +2 more sources
We have described a patient with type 4 Ehlers-Danlos syndrome who died of a ruptured pulmonary artery. Of the six subtypes of Ehlers-Danlos syndrome, which can usually be clinically differentiated, only types 1 and 4 appear to be associated with a substantial risk of arterial rupture.
W, Pearl, M, Spicer
openaire +2 more sources
Postural tachycardia syndrome and other forms of orthostatic intolerance in Ehlers-Danlos syndrome
Autonomic Neuroscience: Basic and Clinical, 2018 Objective: To review the association between orthostatic intolerance syndromes and both joint hypermobility and Ehlers-Danlos syndrome, and to propose reasons for identifying hereditary connective tissue disorders in those with orthostatic intolerance in
Peter C Rowe +2 more
exaly +2 more sources
Absence of the inferior labial and lingual frenula in Ehlers-Danlos syndrome
Lancet, The, 2001 The diagnosis of Ehlers-Danlos syndrome Is based on distinctive phenotypical characteristics such as hyperelastic skin and hypermobile joints. To date, no congenital physical markers exist for Identifying patients with Ehlers-Danlos syndrome.
Paolo Toti +2 more
exaly +2 more sources
Assessment of gait mechanics and muscle strength in hypermobile Ehlers Danlos Syndrome [PDF]
Clinical BiomechanicsBackground: Hypermobile Ehlers Danlos Syndrome, a heritable connective tissue disorder, is associated with muscle dysfunction, joint subluxations and pain.
Clair Francomano +2 more
exaly +2 more sources