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Excessively loose joints are the hallmark of this EDS type
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∙ 13y ago
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What are the symptoms of Classical type EDS?
The major symptoms involved in EDS classical type are the skin and joints
What was arthrochalasia type EDS called?
It was formerly called EDS type VIIB
What was Vascular type EDS called?
It was formerly called EDS type IV
How is EDS treated?
Medical therapy relies on managing symptoms and trying to prevent further complications. There is no cure for EDS
What happens in the Hypermobility type of EDS?
Excessively loose joints are the hallmark of this EDS type
Is EDS classical type inherited?
EDS classical type is inherited in an autosomal dominant manner
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 the EDS type VI also called?
Kyphoscoliosis type
What are the symptoms for a blood type?
A blood type is not a condition or illness. Therefore, a blood type does not and can not have "symptoms".
When do symptoms of Type 3 Gaucher disease occur?
Symptoms of Type 3 Gaucher disease begin during early childhood with symptoms like Type 1.
Which is a characteristic of a type III pfd?
A Type III PFD will not turn most unconscious wearers face-up
When do symptoms of MPS III first appear?
MPS III is a variable condition with symptoms beginning to appear between ages two and six years of age. The condition is characterized by developmental delay, behavioral problems, and mild physical problems
