Excessively loose joints are the hallmark of this EDS type
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.
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.
It was formerly called EDS type VIIB
It was formerly called EDS type IV
Excessively loose joints are the hallmark of this EDS type
EDS classical type is inherited in an autosomal dominant manner
The major symptoms involved in EDS classical type are the skin and joints
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.
Yes
Hypermobility is when your joints extend further than they are supposed to and it can cause sever chronic(non-stop) pain.
Kyphoscoliosis type
Type II: Severe or hypermobility in the urethra of more than 0.8 in (2 cm), with or without decent of the urethra into pelvic structures.