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Foundation for USP7 Related Diseases Announces Grant to Neurolentech in Search for Cure to Rare Disease Hao-Fountain Syndrome

Share this article Share this article FALMOUTH, Maine, April 5, 2021 /PRNewswire/ The Foundation for USP7 Related Diseases (usp7.org) today announced a new research grant award to Neurolentech in a search for a cure to the rare disease Hao-Fountain Syndrome. The Austrian startup Neurolentech, led by Carsten Pfeffer, Ph.D. and co-founded by Gaia Novarino, Professor for Neuroscience at Institute of Science and Technology Austria (IST Austria), will receive $100,000 over two years towards funding studies that will focus on modeling Hao-Fountain Syndrome in cells.  Group photo of Hao-Fountain families at their most recent conference Hao-Fountain Syndrome is a rare genetic disorder caused by mutations in the USP7 gene, with just 80 known patients worldwide. It leads to autism spectrum disorder, increased prevalence of epilepsy, developmental delay/intellectual disability, abnormal brain MRIs, speech impairment, hypotonia, gastrointestinal issues, and eye anomalies.

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Foundation for USP7 Related Diseases Makes Grant to Neurolentech

Foundation for USP7 Related Diseases Makes Grant to Neurolentech Share Rare Daily Staff The Foundation for USP7 Related Diseases said it awarded a two-year $100,000 grant to Neurolentech in a search for a cure for the rare disease Hao-Fountain syndrome, which is caused by USP7 mutations. The Austrian startup Neurolentech, co-founded by Gaia Novarino, a professor of neuroscience at the Institute of Science and Technology Austria (IST Austria), will receive $100,000 over two years towards funding studies that will focus on modeling Hao-Fountain syndrome in cells. Hao-Fountain syndrome is a rare genetic disorder caused by mutations in the USP7 gene, with just 80 known patients worldwide. It leads to autism spectrum disorder, increased prevalence of epilepsy, developmental delay/intellectual disability, abnormal brain MRIs, speech impairment, hypotonia, gastrointestinal issues, and eye anomalies.

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