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Ehlers-Danlos syndrome (EDS) does not appear to be significantly more common in any specific ethnicity; it affects individuals across all ethnic groups. However, certain genetic variants associated with EDS may be more prevalent in specific populations. Overall, the incidence rates can vary due to differences in genetic backgrounds and reporting practices, but no ethnic group is definitively known to have a higher prevalence of EDS.
What else can I help you with?
What is the life span of a person with Ehlers-Donlos Syndrom?
The life span of individuals with Ehlers-Danlos Syndrome can vary depending on the type and severity of the condition. While certain types may have a normal life expectancy, others that affect major organs like the heart can potentially lead to complications that may affect longevity. It is important for individuals with Ehlers-Danlos Syndrome to receive appropriate medical care and management to address potential health issues.
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
Does ehlers danlos syndrome affect your mouth?
Ehlers-Danlos syndrome can cause sensitive/bleeding gums as well as loose teeth. TMJ, which is a condition characterized by a clicking noise in the jaw, is also common among people with EDS. The jaw may also be easily dislocated and painful. There is also evidence that it can cause an increased rate of cavities.
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).
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.
The India rubber man at the carnival may be suspected of having what disease?
ehlers-danlos syndrome
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 pathophysiology of ehlers danlos syndrome?
Its the defect in your collagen 1,3,4. This affects dermal, vascular, and other systems.
What is the deadliest skin diseases?
Harlequin Ichthyosis Epidermolysis Bullosa Ehlers-Danlos Syndrome Scleroderma Leishmaniasis
