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Coping with a Dual Diagnosis

Parents are usually blindsided when they find out that their child has congenital hyperinsulinism (HI), a rare genetic disorder that depresses blood sugar to dangerously low levels.

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When Anisocoria Signals A Bigger Problem

A 10-month-old female infant was referred to the Neuro-ophthalmology clinic at Children’s Hospital of Philadelphia for a new-onset lid ptosis and pupillary miosis on the right side.

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Revised Criteria Lead To More Accurate Screen For ROP In Premature Infants

A multicenter group of 41 hospitals led by researchers at Children’s Hospital of Philadelphia has confirmed that an improved method for predicting retinopathy of prematurity (ROP) was able to reduce the number of babies having invasive diagnostic examinations by nearly a third, while raising disease detection up to 100%.

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