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.

Ehlers-Danlos syndrome EDS is a group of genetic disorders that affect the connective tissues. Connective tissues are proteins, such as collagen, that provide elasticity and support to the joints, blood vessels, and skin. Most children with EDS have hypermobile joints that are prone to full or partial dislocation. However, there are several causes of hypermobility, and many children with hypermobile joints do not have EDS. Many children with EDS also have soft, fragile skin and bruise easily.

23 signs you grew up with ehlers danlos syndrome

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. Depending on the type of EDS, the faulty gene may have been inherited from 1 parent or both parents. Sometimes the faulty gene is not inherited, but occurs in the person for the first time. The diagnosis is made based on a person's medical history and a physical examination. It affects the blood vessels and internal organs, which can cause them to split open and lead to life-threatening bleeding. Some people have problems caused by hypermobility, but do not have any of the specific EDS conditions. You do not usually need to worry if you only have a few symptoms and they're not causing any problems.

Elsevier; Some symptoms of hEDS are: Hypermobility of joints Unstable joints that tend to dislocate easily Clicking and pain in the joints Easy skin bruising Digestive problems like heartburn Dizziness and increased heart rate after standing up Urinary incontinence There are no diagnostic tests for hEDS. Very interesting and detailed reports.

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.

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

Federal government websites often end in. Before sharing sensitive information, make sure you're on a federal government site. The site is secure. NCBI Bookshelf. Tyler Miklovic ; Vanessa C. Authors Tyler Miklovic 1 ; Vanessa C. Sieg 2. Ehlers-Danlos syndrome EDS is a genetic disorder affecting collagen formation and function.

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The EDS Support UK website has more information about the different types of EDS Hypermobile EDS People with hEDS may have: joint hypermobility loose, unstable joints that dislocate easily joint pain and clicking joints extreme tiredness fatigue skin that bruises easily digestive problems, such as heartburn and constipation dizziness and an increased heart rate after standing up problems with internal organs, such as mitral valve problems or organ prolapse problems with bladder control urinary incontinence Currently, there are no tests to confirm whether someone has hEDS. Learn more about Arteriopathy Program. EDS can affect people in different ways. A few ways to manage Ehler-Danlos syndrome are:. Medical Professionals. Connective tissue is a complex mixture of proteins and other substances that provide strength and elasticity to the underlying structures in your body. The GP may refer you to a joint specialist rheumatologist if you have problems with your joints and they suspect EDS. Page last reviewed: 04 October Next review due: 04 October EDS is a group of genetic disorders that affect the body's connective tissues, which provide support and structure to various organs and systems. Any actions or decisions taken based on this information are the sole responsibility of the user.

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. Ehlers-Danlos symdrome EDS affects your collagen, a connective tissue found everywhere in your body.

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. This connective tissue disorder affects individuals in various ways, impacting their joints, skin, and overall quality of life. There is no cure for Ehler-Danlos syndrome. Different types of Ehlers-Danlos syndrome are associated with a variety of genetic causes, some of which are inherited and passed on from parent to child. Genetic testing can be done for the classical, vascular, kyphoscoliosis, and arthrochalasis types of EDS. Physical therapy: Joints with weak connective tissue in Enhler Danlos increases the risk for dislocations. Let us help you today! Learn more about Orthopedic Center. Kyphoscoliosis EDS: Children with this type typically have severe EDS at birth, delayed motor development, and progressive kyphosis and scoliosis. People with kEDS may have: curvature of the spine — this starts in early childhood and often gets worse in the teenage years joint hypermobility loose, unstable joints that dislocate easily weak muscle tone from childhood hypotonia — this may cause a delay in sitting and walking, or difficulty walking if symptoms get worse fragile eyes that can easily be damaged soft, velvety skin that is stretchy, bruises easily and scars Hypermobility spectrum disorder HSD Some people have problems caused by hypermobility, but do not have any of the specific EDS conditions. Morrow ES Jr.