WebSMARD is genetic disease that is inherited in a recessive pattern. This means that both parents must be carriers of the gene mutation and each parent must pass a copy of the mutation on for the child to affected. This means that every time two carriers have a baby, there is a 1 in 4 or 25% chance they will have an affected baby (see diagram below). WebApr 7, 2024 · Looking toward the future and potential gene therapy for SMARD1. As part of his care, Brooks sees Arpita Lakhotia, M.D., child neurologist with Norton Children’s Neuroscience Institute, affiliated with the UofL School of Medicine.Brooks is seen in the Norton Children’s Neuroscience Institute Neuromuscular Disorders Clinic. “Dr. Lakhotia is …
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