An experimental treatment could be lifesaving for a 6-year-old Castaic boy with a rare genetic disorder, but unless his family is able to raise funding, that research may never get off the ground. Carter Sarkar was diagnosed with Sanfilippo syndrome — sometimes referred to as childhood Alzheimer’s — which is currently considered fatal. But through the Cure Sanfilippo Foundation, his family is hoping he can participate in a potentially groundbreaking clinical trial that could also save his life. The neurodegenerative…
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