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 Ehlers-Danlos is a rare diease and most people will test negative. However, for those who test positive, there have been advancements in vascular EDS treatments and management that can greatly improve outcomes. The first step is taking control of your healthcare so that your doctors and insurance will give you access to those treatments.
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Complications may include aortic dissection, joint dislocations, scoliosis, chronic pain, or early osteoarthritis. 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 alteration, also known as a mutation, in a gene called COL3A1.
If you experience sudden chest, back or abdominal pain, go to a hospital emergency department immediately. Patients with haploinsufficiency vascular EDS have a different underlying cause of their vascular EDS. Most vascular EDS patients have one 'normal' type III collagen gene (COL3A1) and one 'abnormal' (or mutated) type III collagen gene.
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If I do 12/13 hour shifts I am in pain the next day and have to rest all day so my days off are not spent enjoying myself or doing things like chores, just recovering and feeling like a failure Vascular variant of Ehlers–Danlos syndrome. Vascular EDS (formerly categorized as type 4) is identified by skin that is thin, translucent, extremely fragile, and bruises easily.
Distichiasis may range from a few extra lashes to a full set of extra eyelashes. Swelling most often affects both legs (bilateral) and usually occurs around puberty.
Coronary Vascular EDS (vEDS). 756.83. Mar 18, 2019 Associate Professor, Pediatrics – Cardiology. Medical Director, Cardiovascular Genetics. Vascular Ehlers-Danlos syndrome -.
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2017-08-24 · It is generally considered the most severe form of Ehlers-Danlos syndrome (EDS).
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Making a diagnosis of vascular EDS. Distichiasis may range from a few extra lashes to a full set of extra eyelashes. Swelling most often affects both legs (bilateral) and usually occurs around puberty. We are going to talk about the effects of Ehlers-Danlos Syndrome on the visual system. Treatments, as Of course, eyelash growth also happens, and thus the. Ehlers-Danlos Syndrome, Type Iv, Autosomal Dominant; Eds4 Vascular EDS is usually caused by a change (mutation) in the COL3A1 gene.
Leffell DJ, Wolff K ( eds) Fitzpatrick's dermatology in general medicine,
Ehlers–Danlos syndrome: A cause of epilepsy and periventricular heterotopia and eyelashes, in addition to the classical features of EDS.29. Periodontitis type
Ehlers-Danlos syndrome (EDS) is an inherited condition that affects the connective tissues in the body.
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Pregnancy; Some forms of EDS (especially Vascular Type EDS) can cause serious complications such as bleeding or tearing during childbirth or premature births. Any woman who has Ehlers-Danlos syndrome should discuss pregnancy with a doctor who is familiar with EDS and its complications
This leads to abnormal collagen fibers, with 7/8ths of the collagen produced being abnormal. 2005-06-01 · Vascular EDS has an autosomal dominant inheritance pattern, individuals and families must be informed of the 50% risk of transmission to the offspring of affected individuals.