Our family is currently trying to educate ourselves regarding a dual diagnosis for our child. Genetic testing revealed a Centronuclear Myopathy ad, paired with Limb-Girdle Muscular Dystrophy ANOC5. Symptoms were evident by 8 yrs old….. is there anyone out there that has experience with a dual diagnosis like this, and or aware of research to help us with this process?
Hello David, there can be so much to take onboard after a diagnosis [or a presumed one, MD is a tricky thing to corner] … take your time and come back ask questions, we will try and answer them or point you in the right direction.
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