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What happens in the Hypermobility type of EDS?

Updated: 8/19/2019
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GaleEncyofMedicine

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13y ago

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Excessively loose joints are the hallmark of this EDS type

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Q: What happens in the Hypermobility type of EDS?
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What is difference between EDS and ERS?

EDS (Ehlers-Danlos syndrome) is a group of genetic connective tissue disorders that affect the skin, joints, and blood vessels, leading to hypermobility and tissue fragility. ERS (Ehlers-Danlos syndrome hypermobility type) is a subtype of EDS that specifically manifests with joint hypermobility and related symptoms without significant skin or tissue involvement.


What is ehlers danlos 3?

Ehlers-Danlos type 3 is the hypermobility form of the Ehlers-Danlos Syndrome. Affects 1 in 10,000 to 15,000 and is caused by an autosomal dominant or autosomal recessive mechanism. Extreme flexibility is the hallmark of this type. It is one of the most surviable types of EDS.


What was arthrochalasia type EDS called?

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What was Vascular type EDS called?

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What are the symptoms of EDS type III?

Excessively loose joints are the hallmark of this EDS type


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EDS classical type is inherited in an autosomal dominant manner


What are the symptoms of Classical type EDS?

The major symptoms involved in EDS classical type are the skin and joints


Are there distinct facial features in Ehler Danlos type three?

No, there are no distinctive facial features recognized in Ehler Danlos Hypermobility Syndrome (type three.) Recognizable facial features, such as are associated with Marfan's Syndrome, another disorder of the connective tissues, might be useful for diagnosis. Perhaps the nearest thing to a distinct feature for EDS is soft, velvety skin.


Is hypermobility a superpower?

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