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
Ehlers-Danlos is an autosomonal dominant genetic disease. It is passed down from a parent; you are born with it. It involves having defective collagen which affects the way the joints, muscles, organs, and skin function.
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.
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
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.
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.
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.
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.
Dr. Ehlers and Dr. Danlos
classical, hypermobility, vascular, kyphoscoliosis, arthrochalasia, and dermatosparaxis
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).
ehlers-danlos syndrome
Harlequin Ichthyosis Epidermolysis Bullosa Ehlers-Danlos Syndrome Scleroderma Leishmaniasis
Its the defect in your collagen 1,3,4. This affects dermal, vascular, and other systems.