What are the 14 types of Ehlers Danlos?

What are the 14 types of Ehlers Danlos?

Types of Ehlers-Danlos Syndrome

• Arthrochalasia EDS. ...
• Brittle Cornea Syndrome. ...
• Cardiac-Valvular EDS. ...
• Classical EDS. ...
• Classical-like EDS. ...
• Dermatosparaxis EDS. ...
• Hypermobile EDS. ...
• Kyphoscoliotic EDS.

What is the most severe type of EDS?

A more severe form of the disorder, called vascular Ehlers-Danlos syndrome, can cause the walls of your blood vessels, intestines or uterus to rupture.

Can you have two types of Ehlers Danlos?

Q - Can you have more than one type of Ehlers-Danlos syndromes? A - This is extraordinarily rare. It is theoretically possible for a person to inherit one type of EDS from one parent and another type of EDS from the other parent, but in the vast, vast majority of cases a person will only have one type.

What is Ehlers Danlos type 7?

The arthrochalasia type EDS (formerly type VIIa and VIIb) is characterized by severe generalized joint hypermobility with multiple dislocations including congenital bilateral dislocation of the hips, muscular hypotonia and distinct dysmorphic features.

Does Ehlers Danlos get worse with age?

Many of the problems associated with EDS are progressive, meaning that they get worse over time.

Is EDS an autoimmune disease?

A much rarer group of connective tissue disorders is called Ehlers-Danlos syndrome. Unlike the diseases noted above, Ehlers-Danlos syndrome is not an autoimmune condition, it's an inherited disorder.

What is the life expectancy of someone with Ehlers Danlos Syndrome?

People affected by vascular EDS have a median life expectancy of 48 years and many will have a major event by age 40. The lifespan of people with the kyphoscoliosis form is also decreased, largely due to the vascular involvement and the potential for restrictive lung disease.

What is Ehlers-Danlos type 4?

Ehlers-Danlos syndrome type IV, the vascular type of Ehlers-Danlos syndromes (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels on the trunk and lower back, easy bruising, and severe arterial ...

What is Ehlers-Danlos type 6?

The Ehlers-Danlos syndrome type VI (EDSVI) is an autosomal recessive connective tissue disease which is characterized by severe hypotonia at birth, progressive kyphoscoliosis, skin hyperelasticity and fragility, joint hypermobility and (sub-)luxations, microcornea, rupture of arteries and the eye globe, and osteopenia.

Will I end up in a wheelchair with EDS?

Some patients with EDS may require specialized mobility devices, such as a wheelchair or a scooter, and a walker, crutches or a cane for mobility. However, care should be taken so that joints and other areas of the body affected by the disease are not injured by shifting weight when, say, walking with a cane or crutch.

What is the life expectancy of someone with Ehlers Danlos?

• Vascular ehlers danlos syndrome or EDS affected individuals have a medium life expectation of 48 years moreover majority will have a main incident by age forty.

Is Ehlers Danlos contagious?

• Ehlers-Danlos syndrome type VI is not related to infection. About contagion and contagiousness: Contagion and contagiousness refers to how easily the spread of Ehlers-Danlos syndrome type VI is possible from one person to another. Other words for contagion include "infection", "infectiousness", "transmission" or "transmissability".

What is hypermobility syndrome/Ehlers Danlos syndrome?

• Ehlers-Danlos syndrome hypermobility type is a connective tissue disorder that mostly affects the bones and joints. People with this condition have loose joints and frequently have long-term joint pain. What other names do people use for Ehlers-Danlos syndrome hypermobility type?