Does Ehlers Danlos affect the eyes?

Ophthalmological abnormalities in EDS include but are not limited to myopia, retinal detachment and glaucoma. Some of these can be vision-threatening. An optometrist or ophthalmologist should establish a comprehensive baseline for a person with EDS, including a complete eye exam and history.

Can you have EDS and psoriasis?

We found that Ehlers-Danlos type III is highly associated with rheumatological conditions, including RA, psoriasis, PsA, fibromyalgia, etc.

What are 3 of the cardinal features of Ehlers Danlos?

7.2 Ehlers-Danlos Syndrome. EDS is a genetically and clinically heterogeneous heritable disorder characterized by abnormal collagen synthesis, and whose cardinal features include joint hypermobility, skin hyperextensibility, and soft connective tissue fragility [47].

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

Vascular and organ rupture are the two most feared and mortal complications of EDS. They are most common in the vascular and kyphoscoliotic subtypes but have been reported in the more common subtypes as well.

Does EDS make you look old?

Due to the collagen in the skin being extra stretchy, many EDS patients experience a lack of wrinkles as they age. This collagen may help EDS patients look younger and can also cause skin to feel extremely soft. Doctor’s even describe the skin as “velvet-soft”.

Is Fibromyalgia really EDS?

Fibromyalgia (FM) is probably the most common diagnosis given to people with CWP. However Ehlers-Danlos syndrome (EDS) (particularly hypermobile Ehlers-Danlos syndrome (hEDS) and the related hypermobility spectrum disorders (HSD)) can also present with a similar picture.

Do Rheumatologists treat Ehlers-Danlos?

The rheumatologist can play an important role in the diagnosis of EDS and is central to the ongoing management of many EDS patients.

Is Ehlers-Danlos an autoimmune disorder?

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.

At what age is EDS usually diagnosed?

Affected people have extremely fragile, sagging skin. It is usually diagnosed before the age of 2 years.

At what age is EDS diagnosed?

The age at first diagnosis peaked in the age group 5–9 years for men and 15–19 years for women (see figure 2). There was a significant difference of 8.5 years in the mean age of diagnosis between men and women (95% CI: 7.70 to 9.22): 9.6 years in EDS (95% CI: 6.85 to 12.31) and 8.3 years in JHS (95% CI: 7.58 to 9.11).

What does EDS pain feel like?

I was asked recently to describe what my body feels with EDS. I described the feeling of being tenderized with a mallet all over my body. Not enough to break bones, but hard enough to leave bruises. This is my daily experience even with the aid of pain meds.

Why are EDS patients called zebras?

According to the international Ehlers-Danlos Society, the reference to zebras is borrowed from a common expression heard in medicine: “When you hear hoofbeats behind you, don’t expect to see a zebra.” In other words, medical professionals are typically taught to look out for more-common ailments rather than testing for …

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.

When to see an ophthalmologist for Ehlers Danlos?

If Ehlers-Danlos syndrome is suspected, ophthalmological examination can also provide support for the diagnosis. An ophthalmological and orthoptic evaluation should be performed in all patients with Ehlers-Danlos syndrome to detect and treat ocular manifestations.

What are the symptoms of the Ehlers-Danlos syndrome?

Here we briefly report on problems that arise from symptoms like weakness of the ligaments of the neck, back problems, and the weakness of the protective layers around nerves.

How is Strabismus related to Ehlers Danlos syndrome?

Strabismus. Strabismus occurs when the six extraocular muscles that control eye movement are not in balance. Not dissimilar to the loose joints in the Ehlers Danlos Syndrome patient, one or more of the extraocular muscles is looser than the others, resulting in the eye drifting or crossing.

https://www.youtube.com/watch?v=Au5GillheDM