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What are the symptoms of Ehlers Danlos Syndrome?
According to the Mayo Clinic there are a number of things that can be considered symptoms of Ehlers Danlos Syndrome. Some of these symptoms are stretchy and fragile skin, overly flexible joints, and fatty lumps at pressure points.
When was Ehlers-Danlos Syndrome identified?
Hello, I see you are asking "What is 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. For more information, you can visit this URL - skincarehealthcenter. com/condition/ehlers-danlos-syndrome/c/12004
What is Ehlers-Danlos syndrome?
Ehlers=Danlos syndrome is a defect in collagen. The most obvious manifestations i hyperextensible joints ("double jointedness"). It can also cause joint pain and affect other systems, especially the vascular system (blood vessels).
What is the pathology of ehlers-danlos syndrome?
Ehlers-Danlos syndrome is a group of connective tissue disorders characterized by defects in collagen synthesis and structure. This results in hypermobility of joints, skin elasticity, and tissue fragility. It is typically caused by mutations in genes involved in collagen production.
What is the link with toes and ehlers danlos?
With Ehlers-Danlos Syndrome, especially the hypermobility type, your toes, as with most other joints, can be extremely flexible. They can usually be bent back to the top of the foot and are usually very easily dislocated. This is due to the laxity of the ligaments. This can be very painful.
What is ehlers danlos 3?
Ehlers-Danlos type 3 is the hypermobility form of the Ehlers-Danlos Syndrome. Affects 1 in 10,000 to 15,000 and is caused by an autosomal dominant or autosomal recessive mechanism. Extreme flexibility is the hallmark of this type. It is one of the most surviable types of EDS.
What is difference between EDS and ERS?
EDS (Ehlers-Danlos syndrome) is a group of genetic connective tissue disorders that affect the skin, joints, and blood vessels, leading to hypermobility and tissue fragility. ERS (Ehlers-Danlos syndrome hypermobility type) is a subtype of EDS that specifically manifests with joint hypermobility and related symptoms without significant skin or tissue involvement.
Ehlers-Danlos Syndrome may join circus doing what?
This inherited disorder causes extreme flexibility of joints and skin (although it has bad sides too!). In a circus setting I know of one performer who is nicknamed Mr elastic and stretches his skin to shocking lengths, worth a watch if you're interested - youtube it: http://www.youtube.com/watch?v=pEwIBS-A21M.
Why can some people dislocate or separate their sholders on will?
It is possible that they may have a connective tissue disorder such as Ehlers-danlos syndrome or Marfan syndrome. People with such disorders have issues with collagen production which can lead to hyperelastic ligaments and loose joints. Subluxations and dislocations are a hallmark of these disorders.
What cause hyperflexibility?
Hyperflexibility, often referred to as hypermobility, can be caused by genetic factors that affect connective tissue, making it more elastic. Conditions like Ehlers-Danlos syndrome or Marfan syndrome can also lead to increased flexibility in joints. Additionally, certain training and stretching practices can contribute to hyperflexibility, especially in athletes and dancers. Environmental factors and overall physical conditioning may also play a role in developing this trait.
What medical condition could someone that has congenital glaucoma septal defects hernia problems long finger long limbs a simian crease flat foot with bent toes and no mental retardation have?
I would look into EDS (Ehlers-Danlos Syndrome). All those symptoms match. EDS is a connective tissue disorder. It can affect eyes, heart, muscles, and joints. Does any of your joints pop in and out? Or do you have pain in joints? I know when I got the dx of EDS my genetics doctor wanted to look at my feet for flatness and also looks at fingers and limbs. Or Marfans Syndrome would also be a good match.....hope that helps.....
What is the pretty disease I read about it in Seventeen many years ago but don't remember what it's proper name is.?
The name of the disease you are referring to is likely Ehlers-Danlos syndrome (EDS), which is a group of connective tissue disorders that can affect the skin, joints, and blood vessels. People with EDS often have hypermobile joints, stretchy skin, and easy bruising, which may have been described as "pretty" in a magazine like Seventeen due to the unique physical characteristics associated with the condition.
