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In my case, it was my father, who was "double jointed" like me. He was never diagnosed, but died at age 75 of Parkinson's with dementia. I am female and have fibromyalgia in addition to the EDS. I think my 26 year old son has at least the FM, if not the EDS also.

The three most prevalent types of Ehlers-Danlos Syndrome (Hypermobility, Classic, and Vascular) are autosomal dominant defects. This means that they are dominant traits, which are not passed on via the X or Y chromosomes. Being a carrier is only applicable to recessive traits, so for these types of EDS, there really aren't "carriers." You either have an inherited defect that causes EDS, or you don't.

If one parent has one of these three types of EDS, then each child has a 50% chance of inheriting the dominant gene. If both parents have one of these types of EDS, then each child has a 75% overall chance of inheriting a type of EDS (a 50% chance of inheriting one or the other, and a 25% chance of inheriting both defects).

Some of the more rare forms of EDS are inherited recessively, so one can be a carrier of these. However, with about 100 total cases identified of these rare forms, it's very unlikely that any one person will be a carrier of these.

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Q: Who is a carrier of Ehlers-Danlos Syndrome?
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