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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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Headache in Ehlers—Danlos Syndrome
Cephalalgia, 1999Objective: Ehlers—Danlos Syndrome (EDS) is a complex hereditary connective tissue disorder with neurologic manifestations that include cerebrovascular disorders and chronic pain. The clinical data collected on 18 patients with EDS and chronic headaches is reported.
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Localized Ehlers-Danlos Syndrome
Archives of Dermatology, 1979A 34-year-old woman had the cutaneous features of the Ehlers-Danlos syndrome, which was strictly limited to the skin and subcutaneous tissue in the region of the left shoulder. The disorder started at approximately age 22 with the development of subcutaneous nodules.
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Ehlers‐Danlos syndrome and delivery
Acta Obstetricia et Gynecologica Scandinavica, 1994Ehlers‐Danlos syndrome (EDS) comprises a group of heritable disorders of connective tissue. The present classification comprises ten or more types, based on a combination of clinical, genetic and biochemical criteria (1). The inheritance is usually autosomal dominant, but rarely recessive and X‐linked recessive cases occur.
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2008
Ehlers-Danlos syndrome (EDS) is an umbrella term which encompasses a heterogeneous group of connective tissue disorders with distinct inheritance patterns, biochemical defects, and prognostic implications (Byers 1997, Beighton et al. 1998, Yeowell et al. 1993). Clinically, this group of disorders is collectively characterised by fragile or hyperelastic
Salvatore Savasta, Maurizia Valli
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Ehlers-Danlos syndrome (EDS) is an umbrella term which encompasses a heterogeneous group of connective tissue disorders with distinct inheritance patterns, biochemical defects, and prognostic implications (Byers 1997, Beighton et al. 1998, Yeowell et al. 1993). Clinically, this group of disorders is collectively characterised by fragile or hyperelastic
Salvatore Savasta, Maurizia Valli
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Celiprolol Treatment in Patients with Vascular Ehlers-Danlos Syndrome
European Journal of Vascular and Endovascular Surgery, 2021Martin Bjorck +2 more
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