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Pallister-Killian Syndrome

<p>Pallister-Killian syndrome is a rare genetic disorder characterized by weak muscle tone, distinct facial features, intellectual impairment, developmental delays, and other systemic involvement.</p>

Children’s Hospital of Philadelphia Awarded Inaugural Collaborative Research Grant to Support New Treatments for Cystic Fibrosis

Jun 5, 2024

Researchers from Children’s Hospital of Philadelphia (CHOP), the University of Iowa and the Rochester School of Medicine and Dentistry were awarded a Collaborative Grant today from Emily’s Entourage (EE), an innovative nonprofit that accelerates research for new therapies and a cure for individuals with cystic fibrosis (CF) who don’t benefit from existing treatments.

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