What is the difference between EDS and POTS?
BACKGROUND: POTS is a common form of orthostatic intolerance with an unknown incidence across various ages. EDS is a heterogeneous group of inherited abnormalities of connective tissue characterized by skin hyper-extensibility, joint hypermobility, and connective tissue fragility.
What mimics Ehlers-Danlos Syndrome?
Tnxb−/− mice showed progressive skin hyperextensibility, similar to individuals with Ehlers–Danlos syndrome. Biomechanical testing confirmed increased deformability and reduced tensile strength of their skin.
How does Ehlers-Danlos affect the brain?
Vascular EDS patients are at risk of aneurysms in the aorta (the main artery that carries blood from the heart), and some studies have found that they are also at increased risk of brain aneurysms. Headaches. People with EDS have a higher rate of migraine headaches than the general population.
Can POTS cause leg weakness?
Brief Summary: POTS patients seem to experience orthostasis-dependent muscle weakness and pain as well as increased muscle fatigue upon physical activity, which can be improved by regular aerobic exercise.
Is Ehlers Danlos autoimmune?
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.
How is pots and Ehlers Danlos syndrome related?
PoTS and Ehlers Danlos Syndrome Combined Many people with Ehlers-Danlos syndrome (EDS) suffer from postural orthostatic tachycardia syndrome, a type of dysautonomia (POTS). Dysautonomia is a common disease of the autonomic nervous system, which is in charge of the body’s automatic functions such as digestion, heart rate, sweating, and breathing.
What are the symptoms of Ehlers Danlos ( eds )?
Malfunctioning of the part of the nervous system that controls involuntary bodily functions (e.g. breathing, heart rate) is common with hypermobile EDS. Symptoms include fast heart rate coupled with low blood pressure, digestive and bladder problems, and temperature and sweating dysregulation.
What are the symptoms of EDS and pots?
EDS affects approximately 33% of people with POTS. POTS can be very crippling. Shortness of breath and headaches are just a few of the symptoms of POTS. Standing causes nausea or extreme cramping for certain people, including myself.
What happens if you have hypermobile Ehlers Danlos syndrome?
If you have the most common form, hypermobile Ehlers-Danlos syndrome, there’s a 50% chance that you’ll pass on the gene to each of your children. Complications depend on the types of signs and symptoms you have. For example, overly flexible joints can result in joint dislocations and early-onset arthritis.