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2013
The Ehlers-Danlos Syndromes comprise a heterogeneous group of diseases, which are characterized by fragility of the soft connective tissues and widespread manifestations in skin, ligaments and joints, blood vessels and internal organs. The clinical spectrum varies from mild skin and joint hyperlaxity to severe physical disability and life-threatening ...
Fransiska, Malfait, Anne, De Paepe
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The Ehlers-Danlos Syndromes comprise a heterogeneous group of diseases, which are characterized by fragility of the soft connective tissues and widespread manifestations in skin, ligaments and joints, blood vessels and internal organs. The clinical spectrum varies from mild skin and joint hyperlaxity to severe physical disability and life-threatening ...
Fransiska, Malfait, Anne, De Paepe
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Archives of Pediatrics & Adolescent Medicine, 1950
The syndrome of Ehlers and Danlos apparently is a constitutional dyscrasia of the mesenchyma, characterized by specific manifestations in the skin, joints and subcutaneous tissue, often associated with other congenital defects. Its history was initiated in 1899 when Ehlers reported on a patient to the Danish Dermatologic Society.1With the turn of the ...
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The syndrome of Ehlers and Danlos apparently is a constitutional dyscrasia of the mesenchyma, characterized by specific manifestations in the skin, joints and subcutaneous tissue, often associated with other congenital defects. Its history was initiated in 1899 when Ehlers reported on a patient to the Danish Dermatologic Society.1With the turn of the ...
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Der Hautarzt, 1999
The Ehlers-Danlos syndrome (EDS) comprises a heterogenous group of nine hereditary connective tissue disorders, characterized by hyperelasticity of skin and hypermobility of joints to differing extents. The skin is easily injured and wound healing is delayed. The majority of EDS patients belong to EDS-types I-III. The pathogenesis in these cases is not
J, Brinckmann +5 more
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The Ehlers-Danlos syndrome (EDS) comprises a heterogenous group of nine hereditary connective tissue disorders, characterized by hyperelasticity of skin and hypermobility of joints to differing extents. The skin is easily injured and wound healing is delayed. The majority of EDS patients belong to EDS-types I-III. The pathogenesis in these cases is not
J, Brinckmann +5 more
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Ehlers-Danlos Syndrome in Athletes
Current Sports Medicine Reports, 2006Ehlers-Danlos syndrome (EDS) should be considered in the evaluation of the hypermobile athlete. EDS is a group of inheritable connective tissue disorders affecting collagen and is characterized by articular hypermobility, skin extensibility, and tissue fragility.
Erik L, Schroeder, Mark E, Lavallee
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Pneumothorax in the Ehlers-Danlos syndrome
Irish Journal of Medical Science, 1981The paucity of descriptions of pneumothorax in association with the Ehlers-Danlos syndrome has led to the assertion that the association is coincidental rather than a consequence of the underlying connective tissue disorder. We report such an association and suggest that its true incidence may be much higher than previously thought due to the wide ...
S, O'Neill +3 more
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Vascular Ehlers–Danlos syndrome
Annales de Génétique, 2004Vascular Ehlers-Danlos syndrome, also known as Ehlers-Danlos syndrome type IV, is a life-threatening inherited disorder of connective tissue, resulting from mutations in the COL3A1 gene coding for type III procollagen. Vascular EDS causes severe fragility of connective tissues with arterial and gastrointestinal rupture, and complications of surgical ...
Dominique P, Germain +1 more
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Gastrectomy in Ehlers-Danlos Syndrome
Archives of Surgery, 1968ALTHOUGH patients with Ehlers-Danlos syndrome have had successful surgery for atrial septal defect, 1 limb amputation, 2 and thoracoplasty, 3 the disease has an historical reputation for both hemorrhagic tendency and wound disruption. 4 Uncontrolled gastrointestinal hemorrhage and wound separation have occurred after appendectomy, 5 but there has been ...
L E, Pierce, M E, Tyrrell, C E, Day
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The radiology of the Ehlers-Danlos syndrome
Clinical Radiology, 1969100 patients with the Ehlers-Danlos syndrome have been investigated clinically; of these 35 were subjected to routine chest x-rays and radiography of clinical abnormalities. A classification of the radiological abnormalities associated with the Ehlers-Danlos syndrome is presented based on our own experience and on reported cases.
P, Beighton, M L, Thomas
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Ehlers-Danlos syndromes and Marfan syndrome
Best Practice & Research Clinical Rheumatology, 2008Ehlers-Danlos syndromes (EDS) and Marfan syndrome (MFS) are multisystemic disorders that primarily affect the soft connective tissues. Both disorders have benefited from recent advances in clinical and molecular characterization, allowing improvements in clinical diagnosis and management.
Bert, Callewaert +3 more
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The vascular ehlers-danlos syndrome
Current Treatment Options in Cardiovascular Medicine, 2006Vascular Ehlers-Danlos syndrome (EDS) is a life-threatening inherited disorder of connective tissue causing severe arterial and gastrointestinal fragility and rupture, as well as complications of surgical and radiologic interventions. The diagnosis should be considered in patients under the age of 45 years who present with arterial tearing or ...
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