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Recent research at Tulane University has unveiled a critical link between a variant of the MTHFR gene, folate deficiency, and hEDS. This deficiency disrupts the binding of crucial proteins to collagen, leading to more elastic connective tissue. This breakthrough could lead to more accurate diagnoses through blood tests and genetic screening​.
POTS can be misdiagnosed for several reasons. Patients may present with various symptoms on multiple occasions, often with no obvious clinical findings.
What is Ehlers Danlos Syndrome Type 3 (hEDS)? Ehlers-Danlos Syndrome (EDS) is a diverse group of congenital disorders characterized by
Overview Those with Ehlers-Danlos syndrome (EDS), have a rare condition that causes weakness in the connective tissue that gives structure
EDS involves hypermobility in joints of elbows, knees, toes, fingers, skin problems, easy bruising of the skin, long-term pain in muscles and bones that are non-responsive to regular pain killers.
The pain was beginning to become ridiculous. I have not ever had any symptoms which I would have interpreted as
The major varieties of Ehlers-Danlos syndrome (EDS) are classified based on the indicators and symptoms that are manifested. It is
Ehlers-Danlos Syndrome represents a complex interplay of genetic, physical, and environmental factors. Early and accurate diagnosis is crucial in managing the diverse manifestations of EDS and improving the quality of life for those affected. Ongoing research and awareness are vital in unraveling the intricacies of EDS and providing better care for patients.