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I also have vascular insufficiency, which my grandmother also suffered from. It was bad enough to warrant being tested for EDS 4 (VEDS) which thankfully came back negative. I have since found a double blinded clinically tested supplement that reduces the painful swelling associated with my vascular insufficiency and is helping to support my veins. Vascular Ehlers-Danlos syndrome (EDS), formerly known as EDS type IV, is an autosomal dominant disorder characterized by fragility of medium and large arteries due to type III procollagen deficiency.

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The frequency is estimated as 1/50,000-1/200,000 and results from pathogenic variants in COL3A1, which encodes the chains of type III procollagen, a major protein in vessel walls and hollow organs. Ehlers-Danlos syndrome comprises a heterogeneous group of collagen disorders (hereditary connective tissue disease). Epidemiology There is a recognized male predominance. Clinical presentation Ehlers-Danlos syndrome clinically manifests with I also have vascular insufficiency, which my grandmother also suffered from.

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Vascular EDS is particularly serious because of the risk for spontaneous arterial or organ rupture. Vascular EDS is estimated to occur between 1 in 50,000 individuals to 1 in 200,000 and results from pathogenic variants in COL3A1, which is responsible for producing chains of type III procollagen, a major protein in the walls of blood vessels Ehlers-Danlos syndrome, vascular type (also known as EDS IV) is characterized by thin, translucent skin; easy bruising; characteristic facial appearance; and arterial, intestinal and/or uterine fragility significant medical problem by age 20 years and more than 80% by age 40 years.

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Vascular Ehlers-Danlos syndrome (vEDS) is a condition that is quite variable. People are often diagnosed when they have easy and frequent bruising that is not explained by other causes, a spontaneous bowel, or arterial tears, or because other family members are affected.

What Vascular EDS Patients are Saying: The symtoms and percentages listed below are from the informal online survey I’ve had posted for a few weeks now. These results are only for the patients who identified themselves or their loved ones as having the Vascular type of Ehlers-Danlos Syndrome. Vascular Disease includes any condition that affects your circulatory system, such as peripheral artery disease. This ranges from diseases of your arteries, veins and lymph vessels to blood disorders that affect circulation.
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It is caused by a gene mutation affecting a major protein, which causes weakness in vessel walls and hollow organs.

Keratoconus – A Common Ocular Complication of Ehlers-Danlos Syndrome In this condition, the cornea (the front part of the eye) bulges outward in a cone shape, and gravity pulls the cone downward, blurring the vision and making it difficult to see well with glasses or soft contact lenses. Vascular Ehlers-Danlos syndrome (vEDS, VEDS, previously known as EDS type IV) is an uncommon, dominantly inherited, genetic connective tissue disorder. Vascular EDS is particularly serious because of the risk for spontaneous arterial or organ rupture. Vascular EDS is estimated to occur between 1 in 50,000 individuals to 1 in 200,000 and results from pathogenic variants in COL3A1, which is responsible for producing chains of type III procollagen, a major protein in the walls of blood vessels Ehlers-Danlos syndrome, vascular type (also known as EDS IV) is characterized by thin, translucent skin; easy bruising; characteristic facial appearance; and arterial, intestinal and/or uterine fragility significant medical problem by age 20 years and more than 80% by age 40 years.
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Figure 2. leg was encompassed by a marbled, plum-colored vascular.

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For information on Vascular Ehlers-Danlos syndrome (VEDS), please visit The VEDS Movement, a division of The Marfan Foundation, at thevedsmovement.org.The VEDS Movement offers medical information, support, and more.For more information, please contact Katie Wright, director of The VEDS Movement, at kwright@thevedsmovement.orgTHE VEDS MOVEMENT WEBSITE Vascular Ehlers-Danlos syndrome is a rare, life-threatening, autosomal dominant variant of EDS, resulting from mutations in COL3A1 gene. Affected individuals are prone to serious and potentially fatal complications, especially vascular, intestinal, and uterine ruptures.

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Aug 4, 2017 - Vascular EDS is a life threatening connective tissue disorder that affects all tissues, arteries and internal organs making them extremely fragile. Patients are at risk of sudden arterial or organ rupture. Vascular EDS is a genetic condition caused by an … Hello, I have a diagnosis of hypermobile EDS made clinically with no genetic testing, however two of my family members have features suggestive of vascular EDS (early prominent varicose veins, gingival recession, translucent skin, aortic aneurism (asymptomatic), easy … VEDS- my life x. 495 likes. living with vascular Ehlers-Danlos syndrome. 2007-07-19 Posts about vascular eds written by anunstickysituation.

It most often occurs where the eyelashes grow. Dandruff-like debris builds up at Apr 15, 2014 If you can count more than one row of eyelashes or even just a few Ehlers- Danlos syndrome, a connective tissue disorder that can lead to The Ehlers-Danlos Society creates resources for those with EDS and Zachary shares his story with vascular EDS (vEDS) this #RareDiseaseDay. "Finally by most often vascular or demyelinating, in the dorsal tegmentum of the caudal pons involving the Fitzgerald MJT, Gruener G, Mtui E, eds. strabismus • Marked photophobia • Eyelashes and eyebrows are white • Optic atrophy • Cataract av M Al Haj · 2013 · Citerat av 1 — Dromedaries are noted for their thick eyelashes and small, hairy ears. the Angiotensin II AT1 receptor blocker losartan on vascular and neuro-hormonal In: Robertson JIS, Nicholls MG, Eds. The renin angiotensin system.