Feb 6, 2019 | Diagnosis, Stories
Jori and Dan have a very unique son named Luxton. He is one of three cases in the world that has autosomal recessive centronuclear myopathy type 5. Luxton however is the only one in the world that has two mutated genes. Autosomal Recessive Centronuclear Myopathy...
Mar 4, 2017 | Polymicrogyra, Stories
When Laura wasn’t meeting developmental milestones, Keven and Phyllis brought her their pediatrician. They were shocked to learn that she had polymicrogyria. Over the years they realized what an absolute joy to Laura was to have in their...
