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Its the defect in your collagen 1,3,4.

This affects dermal, vascular, and other systems.

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Q: What is the pathophysiology of ehlers danlos syndrome?
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Who discovered ehlers-danlos syndrome?

Ehlers-Danlos Syndrome was discovered by Edvard L. Ehlers, a Danish dermatologist who first discovered the disease in 1901. Henri-Alexandre Danlos, a French dermatologist published his own description of the disease in 1908.


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


Is there any treatment for ehlers-danlos syndrome?

There is no specific treatment for Ehlers-Danlos Syndrome beyond pain management. For some individuals, protective bracing of limbs and very gentle physical therapy can be effective.


What is Ehliers-danlos syndrome dermatosaraxis?

Ehlers-Danlos syndrome is an inherited connective tissue disorder. It is caused by a defect in the structure, production, and processing of collagen or proteins.


Who are Ehlers-Danlos syndromes named for?

Dr. Ehlers and Dr. Danlos


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 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.


How is Ehlers-Danlos Syndrome divided?

classical, hypermobility, vascular, kyphoscoliosis, arthrochalasia, and dermatosparaxis


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).


The India rubber man at the carnival may be suspected of having what disease?

ehlers-danlos syndrome


What is the deadliest skin diseases?

Harlequin Ichthyosis Epidermolysis Bullosa Ehlers-Danlos Syndrome Scleroderma Leishmaniasis


What doctors in the US specialize in Ehlers Danlos Syndrome?

Dr. Brad Tinkle in Cincinnati OH is a geneticist specializing in EDS and Marfan syndrome.