What are the different types of Ehlers-Danlos syndrome?

There are six types of Ehlers-Danlos (EDS): three main types and three rarer. The most common are hypermobility, classic and vascular, while Cyphoscoliiosis, arthrochalase and dermatosparax are so rare that less than 100 cases of each have been reported. Originally, scientists have recognized 10 types of Ehlers-Danlos syndrome, but the simpler classification of six was introduced in 1997. It is possible that there are more than six recognized types of Ehlers-Danlos syndrome, but these types were found only in specific families and are not well defined or understood.

The most common of the six types of Ehlers-Danlos syndrome is hypermobility, formerly type III. This type EDS is influenced by approximately one in 10,000 to 15,000 people. Typical symptoms include free and unstable joints, muscle fatigue and easy bruises. The instability of the joint causes frequent dislocation that can lead to chronic degenerative joint diseases and premature osteoarthritis. Beeshop is not necessarily the same as having this type EDS. UPatients are also available free joints and muscle fatigue, but the distinctive symptoms are related to the skin. The skin is extremely elastic and fragile. The patient will easily bruise and scar, slowly recover from the wounds and has other skin folds in areas such as eyelids. Oily bearings are common on forearm and shaving, while elbows and knees develop fibrous growth.

The least common of the main types of Ehlers-Danlos is a vascular type, formerly type IV. Although it is rare, affecting about one in 100,000 to 200,000 people, it is one of the most serious types because it affects blood vessels and organs. Blood vessels and organs are easily fragile and easily cracked. The skier is almost translucent and the face usually has a characteristic appearance of protruding eyes, sunken faces and thin nose and lips. Many of these patients may develop problems with collapsed pulmonary and heart valves.

Three remaining types of syndaOmu ehlers-danlos are very rare and affects every less than 100 people. Kyphos Wheel is characterized by severe scoliosis and fragile eye gloracs. Patients with Arthrochalsia will be short and seriously limited by free joints and resulting dislocations. Signs of dermatosparax are very fragile and flabby skin. Other possible types were primarily found in individual families and must be fully defined.

Although six types of Ehlers-Danlos syndrome are well defined, individual cases often resist categorization. It may overlap certain symptoms that lead to diagnosis or incorrect diagnosis. The treatment is largely limited to the relief of symptoms, since since 2011 there is no treatment for this syndrome. Individuals with ED who plan to have children should consult with a genetic advisor before concept.

ED type can determine the prognosis and outlook of the patient. The severity of the symptoms differs significantly between the types of Ehlers-Danlos syndrome. Although most patients may expect to live normalLifetime, some will have mild symptoms, while others will be seriously restricted. EDS is a lifelong problem, but the fear of pain and degeneration can be of the same size or greater burden than physical symptoms.