How long can you live 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.

Who does Ehlers-Danlos syndrome affect the most?

The combined prevalence of all types of Ehlers-Danlos syndrome appears to be at least 1 in 5,000 individuals worldwide. The hypermobile and classical forms are most common; the hypermobile type may affect as many as 1 in 5,000 to 20,000 people, while the classical type probably occurs in 1 in 20,000 to 40,000 people.

What symptoms are associated with Ehlers-Danlos syndrome?

Main types of Ehlers-Danlos syndromes (EDS)

• joint hypermobility.
• loose, unstable joints that dislocate easily.
• joint pain and clicking joints.
• extreme tiredness (fatigue)
• skin that bruises easily.
• digestive problems, such as heartburn and constipation.
• dizziness and an increased heart rate after standing up.

What is the most severe form of Ehlers-Danlos syndrome?

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.

What are the symptoms of classical Ehlers Danlos syndrome?

Classical Ehlers-Danlos syndrome (EDS) is a genetic connective tissue disorder that is caused by defects in a protein called collagen. Common symptoms include skin hyperextensibility, abnormal wound healing, and joint hypermobility.

How to diagnose hypermobile Ehlers Danlos syndrome ( hEDS )?

Diagnostic Criteria for Hypermobile Ehlers-Danlos Syndrome (hEDS) This diagnostic checklist is for doctors across all disciplines to be able to diagnose EDS Patient name: Distributed by The clinical diagnosis of hypermobile EDS needs the simultaneous presence of all criteria, 1 and 2 and 3. DOB: DOV: Evaluator: v9

Are there any alternative diagnoses for Ehlers Danlos?

Alternative diagnoses and diagnostic categories include, but are not limited to, neuromuscular disorders (e.g. Bethlem myopathy), other hereditary disorders of the connective tissue (e.g. other types of EDS, Loeys-Dietz syndrome, Marfan syndrome), and skeletal dysplasias (e.g. osteogenesis imperfecta).

Are there any ocular complications of Ehlers Danlos syndrome?

Common Ocular Complications of Ehlers Danlos Syndrome. Ocular Manifestations of Ehlers-Danlos Syndrome. There is an amazing amount of collagen in the eye (80% of the ocular structures), but relatively, a surprising lack of vision-threatening Ehlers-Danlos Syndrome (EDS) related effects.