23 signs you grew up with ehlers danlos syndrome

Ehlers-Danlos syndrome EDS is a group of genetic disorders that affect the connective tissues.

Connective tissues are made up of proteins and other substances that provide them with elasticity. In people with Ehler-Danlos syndrome, the strength of collagen is affected. Though people with Ehler-Danlos syndrome are born with the condition, it may take years before it gets diagnosed. Ehler-Danlos syndrome is a genetic condition. Over 20 genes have been found to be associated with EDS. Changes variants in these genes may disrupt the production or processing of collagen, resulting in weak bones, skin , or other parts of the body. While for some, it may be related to an underlying medical condition, these may be signs of Ehler-Danlos syndrome for a few people.

23 signs you grew up with ehlers danlos syndrome

Ehlers-Danlos syndrome is a group of inherited disorders that affect your connective tissues — primarily your skin, joints and blood vessel walls. Connective tissue is a complex mixture of proteins and other substances that provide strength and elasticity to the underlying structures in your body. People who have Ehlers-Danlos syndrome usually have overly flexible joints and stretchy, fragile skin. This can become a problem if you have a wound that requires stitches, because the skin often isn't strong enough to hold them. A more severe form of the disorder, called vascular Ehlers-Danlos syndrome, can cause the walls of your blood vessels, intestines or uterus to rupture. Because vascular Ehlers-Danlos syndrome can have serious potential complications in pregnancy, you may want to talk to a genetic counselor before starting a family. There are many different types of Ehlers-Danlos syndrome, but the most common signs and symptoms include:. Symptom severity can vary from person to person and depends on the specific type of Ehlers-Danlos syndrome that you have. The most common type is called hypermobile Ehlers-Danlos syndrome. People who have vascular Ehlers-Danlos syndrome often share distinctive facial features of a thin nose, thin upper lip, small earlobes and prominent eyes. They also have thin, translucent skin that bruises very easily. In fair-skinned people, the underlying blood vessels are very visible through the skin. Vascular Ehlers-Danlos syndrome can weaken your heart's largest artery aorta , as well as the arteries to other regions of your body.

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Back to Health A to Z. Ehlers-Danlos syndromes EDS are a group of rare inherited conditions that affect connective tissue. Connective tissues provide support in skin, tendons, ligaments, blood vessels, internal organs and bones. EDS can affect people in different ways. For some, the condition is relatively mild, while for others their symptoms can be disabling. The different types of EDS are caused by faults in certain genes that make connective tissue weaker.

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23 signs you grew up with ehlers danlos syndrome

Although Ehlers-Danlos syndrome EDS is a condition you are born with, it may take many years or decades before you are diagnosed. There are 13 subtypes of Ehlers-Danlos syndrome, though the hypermobile subtype is the most common. Your symptoms will depend on your subtype , but most people with EDS experience overly flexible joints, regular partial or full joint dislocations while doing everyday activities, stretchy or fragile skin, easy bruising, and chronic pain. We asked our Mighty community to share signs that they grew up with Ehlers-Danlos syndrome , which they can now recognize in retrospect. Perhaps some of these will sound familiar to you, too.

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The genetics specialist will ask about your medical history, family history, assess your symptoms and may carry out a genetic blood test to confirm the diagnosis. Mayo Clinic Alumni Association. When you engage with these links and decide to make a purchase, we may receive a percentage of the sale. Children with vascular EDS may also have short stature, recessed gums, and a low amount of fat under their skin. Turns out I'm deficient in some vitamins and needed to supplement. In-depth results. Ehlers-Danlos syndromes. I ordered one health report from Xcode and received results within an hour. A few ways to manage Ehler-Danlos syndrome are: Medications: Over-the-counter pain-relieving medications are usually the mainstay for EDS treatment. We can help! Cardiovascular Complications : EDS can affect the heart and blood vessels, leading to conditions like mitral valve prolapse and aortic root dilation. Customer Reviews. Kimberlee Jackson. EDS can affect people in different ways. Ferri FF.

For the Ehlers-Danlos syndrome EDS guide, we interviewed three medical experts, read numerous studies and surveyed more than people living with EDS. The guides are living documents and will be updated with new information as it becomes available.

Lower Extremity Program Program The Lower Extremity Program offers comprehensive diagnosis and treatment for children with lower extremity disorders. Mayo Clinic Alumni Association. Physical therapy may be recommended to strengthen muscles and stabilize joints. Request an Appointment Request a Second Opinion. Surgery: Surgery may be required in people with repeated joint dislocations or ruptured blood vessels and organs. Clinical manifestations and diagnosis of Ehlers-Danlos syndromes. Physical therapy: Joints with weak connective tissue in Enhler Danlos increases the risk for dislocations. The Boston Adult Congenital Heart BACH and Pulmonary Hypertension Program offers a full range of inpatient and outpatient clinical services to adults with congenital heart disease and pulmonary hypertension. Community Health Needs Assessment. Ehlers-Danlos syndrome is a complex condition, and your child will likely need care from a range of specialists. Benderson Family Heart Center Center The Benderson Family Heart Center treats the full spectrum of heart disorders, including the rarest and most complex congenital heart defects. This can become a problem if you have a wound that requires stitches, because the skin often isn't strong enough to hold them. All I had to do is upload the data and after a short wait I received all of my reports.