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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>

Neonatal Jaundice: When to Refer

Apr 10, 2017

Newborn jaundice is a common pediatric problem. Most instances are benign, and the challenge for clinicians is to determine when further evaluation is needed.

Giant Cell Myocarditis Required Eventual Transplant

Apr 10, 2017

A case study of a 13-year-old female who was diagnosed with giant cell myocarditis (GCM) and underwent a heart transplant at CHOP. She continues to be monitored for recurrence and signs of rejection.

Sean

A Gift that Speaks for Itself

Apr 4, 2017

For Sean Frankel, the challenge of stuttering was the motivating factor that has driven him to work harder and reach higher. A successful real estate developer, Sean has decided to give back to the place that helped him — and his son.

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