This Vascular Ehlers-Danlos Syndrome management overview provides research papers and publications that may help guide VEDS management for the medical professional. Have a specific question about caring for someone with VEDS? Get connected with an expert.
Some of the features of Vascular Ehlers-Danlos Syndrome (VEDS) are common in the general population; however, treatment is sometimes more complex because of the underlying connective tissue disorder. In addition, there are important considerations because the condition affects multiple body systems.
Diagnosis, natural history, and management in Vascular Ehlers–Danlos Syndrome
Byers, et al. 2017
A multi-institutional experience in Vascular Ehlers-Danlos Syndrome diagnosis
Shalhub, et al. 2019
Spontaneous pneumothorax and hemothorax frequently precede the arterial and intestinal complications of vascular Ehlers-Danlos syndrome.
Shalhub, Neptune, et al. 2019
A multi-institutional experience in the aortic and arterial pathology in individuals with genetically confirmed Vascular Ehlers-Danlos Syndrome.
Shalhub, Byers, et al. 2019
Molecular diagnosis in Vascular Ehlers-Danlos Syndrome predicts pattern of arterial involvement and outcomes.
Shalhub, Black, et al. 2014
Intestinal Perforation in Children as an Important Differential Diagnosis of Vascular Ehlers-Danlos Syndrome
Keon Young Park, et al. 2019
Bowel perforation in type IV Vascular Ehlers-Danlos Syndrome. A systematic review.
El-Masri, et al. 2018
Management of colonic complications of type IV Ehlers-Danlos Syndrome: a systematic review and evidence-based management strategy.
Speake, et al. 2019
Audit of Gastrointestinal Manifestations in Patients with Loeys–Dietz Syndrome and Vascular Ehlers–Danlos Syndrome
Wang, et al. 2020
FDA Warning on the use of Fluoroquinolones
Arterial Complications of vascular Ehlers-Danlos Syndrome
Safety of Endoscopy in Heritable Connective Tissue Disorders
Kilaru, et al. 2019
Iliac Artery Pathology Presentation and Management in Vascular Ehlers-Danlos Syndrome
Shalhub, et al. 2022
Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network for Rare Vascular Diseases (VASCERN)
Michael Frank, et al. 2022
The role of cutaneous manifestations in the diagnosis of the Ehlers‐Danlos syndromes
Burrows, et al. 2022
Endovascular treatment of aortic aneurysms and dissections in patients with genetically triggered aortic diseases
Kolbel et al. 2022
Pain and fatigue in adults with Loeys–Dietz syndrome and vascular Ehlers–Danlos syndrome, a questionnaire‐based study
Heidi et al. 2022
Evaluating perinatal and neonatal outcomes among children with vascular Ehlers–Danlos syndrome
Morris et al. 2022
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