Vascular Ehlers–Danlos syndrome (vascular EDS, vEDS, or VEDS, previously known as Ehlers–Danlos type IV) is a dominantly inherited disorder that results from mutations in COL3A1, the gene that encodes the chains of type III collagen [Pope et al., 1975; Pepin et al., 2014; Frank et al., 2015a].


Vascular EDS is quite rare and is the most severe type of EDS. This type of EDS is very different from hEDS and classic EDS. A doctor who is familiar with EDS can most often tell based on a physical exam and history if someone has vascular EDS.

& al. (eds.) Synonyms key. Bold type = accepted name. Vascular Ehlers-Danlos Syndrome: The Journey Begins: Smith, M J: Books.

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Raven Press, New York, New York 1982: 185  canine proximal fibular epihysis on a vascular pedicle. vascular tensor fascia lata flap and fascia lata. Scand J In: Sjöberg F & Östrup L (Eds): Brännskador. Kurtto, A., Weber, H. E., Lampinen, R. & Sennikov, A. N. (eds.) 2010: Atlas Florae Europaeae. Distribution of Vascular Plants in Europe. 15. Rosaceae (Rubus).

Patients are at risk of sudden arterial or organ rupture.

Objective Vascular Ehlers–Danlos syndrome (vEDS) is a rare genetic condition related to mutations in the COL3A1 gene, responsible of vascular, digestive and  

Även tänder och tandkött kan vara påverkade. Other Medications for Vascular Ehlers-Danlos Syndrome Many physicians suggest routine use of high-dose vitamin C, which can help the body make better use of the collagen that it has available.

Vascular eds

Vi använder medvetet inte förkortningen EDS för denna patientgrupp, utan i stället VED, eftersom vi vill betona de mycket speciella och 

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420 p. Palombi & Partner, Rome. Domina, G. (2011) Plumbaginaceae  av CK Holm · 2017 · Citerat av 1 — kännetecknen för EDS är överrörlighet i leder, töj- bar hud Ehlers-Danlos syndrom (EDS) är en heterogen grupp av bindvävs- of vascular Ehlers-Danlos. Ej kärlskör som EDS men kan vara särskilda problem med fortsatt dilatation events in vascular Ehlers-Danlos syndrome: a prospective, randomized, open,  There are numerous subtypes: classical, hypermobility, vascular, and others. Common clinical features include hyperextensible skin and joints, skin fragility and  Cognitive deficits in preclinical Alzheimer´s disease and vascular dementia: Pat RA, Bäckman L, Nilsson L-G (Eds.) (2004) New frontiers in cognitive aging. Vascular surgery in Sweden as reflected in the Swedish vascular registry (Swedvasc) Angiologiia i sosudistaia khirurgiia = Angiology and vascular surgery.
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Vascular eds

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Some signs of VEDS are easy to see. Every person’s experience with Vascular Ehlers-Danlos syndrome is slightly different. Vascular Ehlers-Danlos syndrome (vEDS) Introduction Vascular EDS (OMIM #130050) is a rare disorder that results from heterozygosity for mutations in COL3A1 which encodes the pro-alpha1 chains of the type III procollagen homotrimer.
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Vascular Ehlers-Danlos Syndrome, or VEDS, is a genetic disorder that affects the body’s connective tissue. Connective tissue holds all the body’s cells, organs, and tissue together. It also plays an important role in helping the body grow and develop properly. Connective tissue is made up of proteins.

This gene controls the production and assembly of type III collagen. Collagen is the most abundant protein found throughout the entire body. For information on Vascular Ehlers-Danlos syndrome (VEDS), please visit The VEDS Movement, a division of The Marfan Foundation, at The VEDS Movement offers medical information, support, and more.

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The Vascular type of EDS is characterized by thin, translucent skin that bruises easily but is not necessarily particularly stretchy, and spontaneous dilation / rupture of arteries and organs (Byers et al, 2017). The problem lies in the production of type 3 collagen. There is also a characteristic facial appearance:

Will you help us give the gift of hope? Our mission is to provide empowering, evidence-based mental health content you can use to help yourself and your loved one Mar 18, 2019 Associate Professor, Pediatrics – Cardiology. Medical Director, Cardiovascular Genetics.