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blood test for mito

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I am asking this to the mito groups...

My sister was diagnosed with M S before we were aware of mito. She has ptosis

and some other symptoms similar to my mito. Her neurologist told her that mito

could be definitively diagnosed with a blood test....Can that be so? Dr.

Shoffner diagnosed my mito with a muscle biopsy. I know he took some blood and

urine also.

Have I missed some new information?

Thanks, in FL

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I'm waiting for my genetic results to see if they find the specific

mutation. I have several people lines up who have neuropathy,

cognitive issues, and muscle weakness in my family, and I would want

my kids screened.

Dr. Shoffner doesn't think my mitochondrial defect is mtDNA, it's

probably nDNA. I have paternal relatives with similar symptoms, so

it will be interesting to see if they carry the same defect.

Take care,

RH

> >

> > >I am asking this to the mito groups...

> > >My sister was diagnosed with M S before we were aware of mito.

> She has ptosis and some other symptoms similar to my mito. Her

> neurologist told her that mito could be definitively diagnosed with

> a blood test....Can that be so? Dr. Shoffner diagnosed my mito

with

> a muscle biopsy. I know he took some blood and urine also.

> > >Have I missed some new information?

> > >Thanks, in FL

> > >

> > >

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