05/31/2026
Welcome Back Everyone!
Today I Present to You...
More Information (My Part Two) About...
Ehler's - Danlos Syndrome Awareness Month!
One Important Note About Ehler's-Danlos Syndrome (EDS),
Is that "Connective Tissue Proteins" are Affected due to Certain "Gene Changes," or "Genetic Mutations," are Passed Down or Inherited by One or Both Biologic Parents to their Biologic Children.
Inherited How You Ask...
There are Two Ways...
Autosomal Dominant Inheritance:
You Only Need One Copy of the Gene Change (Mutation) Located on a Non-Sex (Gender) Chromozone to Inherit the Condition. (One Parent may or may not Show Signs or Symptoms themselves)
Autosomal Recessive Inheritance:
You Need Two Copies of the Gene Change (Mutation) Located on a Non-Sex (Gender) Chromozone to Inherit the Condition. (Both Parents DO NOT Show Signs or Symptoms Themselves, Both Parents are Carriers of the Gene Change (Mutation).
Knowing how Ehler's - Danlos Syndrome was Inherited is a Start to Understanding the 13 Types Ehler's-Danlos Syndrome.
1) Hypermobile Ehler's-Danlos Syndrome (hEDS)
2) Classical Ehler's-Danlos Syndrome (cEDS)
3) Vascular Ehler's-Danlos Syndrome (vEDS)
4) Kyphoscoliotic Ehler's-Danlos Syndrome (kEDS)
5) Arthronchalasia Ehler's-Danlos Syndrome (aEDS)
6) Dermatospraxis Ehler's-Danlos Syndrome (dEDS)
7) Brittle Cornea Syndrome (BCS)
8) Musculocontractural Ehler's-Danlos Syndrome (mcEDS)
9) Spondylodysplastic Ehler's-Danlos Syndrome (spEDS)
10) Periodontal Ehler's-Danlos Syndrome (pEDS)
11) Myophathic Ehler's-Danlos Syndrome (mEDS)
12) Classic-Like Ehler's-Danlos Syndrome (clEDS)
13) Cardiac-Vasccular Ehler's-Danlos Syndrome (cvEDS)
*Each Type (1-13) come with Its Own Set of Symptoms and Causes. *
I will let you take a long, I Mean LOONNNGGGG Look at This Information to Absorb or Understand it. I Know It is A LOT... Take Your Time...
Yours,
Robin @ The Nebula Palace
