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Who are Ehlers-Danlos syndromes named for?
Dr. Ehlers and Dr. Danlos
When did Henri-Alexandre Danlos die?
Henri-Alexandre Danlos died in 1912.
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.
What are the Ehlers-Danlos syndromes?
The Ehlers-Danlos syndromes (EDS) refer to a group of inherited disorders that affect collagen structure and function
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.
How many people get ehlers-danlos each year?
Ehlers Danlos Syndrome is not a terminal disease, but an inherited disorder of the connective tissue throughout the body. Although individuals with EDS may experience chronic pain and disability, their life expectancy is the same as anyone's.
How common are Ehlers-Danlos syndromes?
Today, according to the Ehlers-Danlos National Foundation, one in 5,000 to one in 10,000 people are affected by some form of EDS
Where is the Ehlers-Danlos Support Group-UK?
Farnham, Surrey
Where is the Elhers-Danlos National Foundation?
Los Angeles, CA
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 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
