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Cutis hyperelastica is a genetic mutation of the fibrous tissue creating connective collagen. The condition is not necessarily passed on, and can simply be caused from a mutation of the gene on an individual basis. However the gene is recessive and can be passed on from parent to child. Only one parent is required to carry the mutated gene to cause the disorder.
The odds of the mutation being passed and showing symptoms is somewhat unknown, there are many types are Cutis hyperelastica so inheritance patterns vary.
While the condition can indeed occur from a spontaneous mutation, the defects that cause the three most prevalent forms of Ehlers-Danlos Syndrome (hypermobility, classic, and vascular) are autosomal dominant, meaning that the defect requires only one parent to possess it and that it is not passed on the sex (X/Y) chromosomes. The more rare forms (~100 total cases identified, worldwide) are recessive defects.
Prevalence rates for the three most prevalent forms are currently estimated at
- Hypermobility Type: about 1 in 10,000 to 15,000 people
- Classic Type: about 1 in 20,000 to 50,000 people
- Vascular Type: about 1 in 100,000 to 250,000 people
What else can I help you with?
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
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 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 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
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.
