My son is 7 years old and has had symptoms his whole life. He was finally clinically diagnosed with Hereditary Sensory Autonomic Neuropathy on Friday. We know that he doesn't have a known phenotype.

The diagnosis was made via nerve biopsy and clinical symptoms. He has stripping of his myelin sheathing.

His symptoms include significant dysmotility, reverse motility, autonomic dysfunction, central sleep apnea, connective tissue issues, and color blindness. There are other issues but those are the major issues.

We have looked for many years and he has stumped doctors. I wasn't expecting an answer this week and so am in a little shock that we have at least a physiological understanding of what is going on.

We will be going through whole exome sequencing to find the genetic marker for my son's disease.

Does anyone else have HSAN that does not fall into the typical forms?

Thanks,

Yael

I check into Neurotalk every once in a while, but today my "issues" aren't important. This site has been a great source of info for me and you become connected to strangers as you seek your own answers. Blessings and hugs today from a "stranger" who hopes the answers for your son will result in comfort for you all, both physically, mentally and spiritually.

yweinst,

It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. Please, just let us know how we can help you out. You will find out we are supportive and relaxing place.

Looks like you found the PN forum. There will be a great deal of friends to help you out.

Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.

I am so sorry - he is so young. My daughter was diagnosed this year with a previously undocumented DNMT1 variant of HSAN. She is 32 years old. I have never read of a case as young as your son. I have a lot of questions of course, but this is my first time on a group like this and I feel a bit awkward about seeming nosy. It has taken almost 8 years for Emma to get a diagnosis. It has been enormously frustrating. We have been lucky this last year - luck!! - to have found a doctor at the Mayo Clinic who specializes in DNMT1 variant research. He has helped clarify a lot for us.

It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. Please, just let us know how we can help you out. You will find out we are supportive and relaxing place.

Click on the following forum for some assistance, there are some wonderful friends for you.

Peripheral Neuropathy:
http://neurotalk.psychcentral.com/forum20.html

Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.

Welcome .. I know you will get support, help and sympathy on this board .. And we Ll need that at times.