A imaging test to detect cancer and neurological diseases, using special pictures taken after a tiny amount of a radioactive liquid is injected into a vein.

An acronym for the syndrome: Posterior fossa malformations, Hemangioma, Arterial anomalies, Cardiac anomalies, Eye abnormalities, and Sternal clefting and supraumbilical raphe.

PHOX2B gene testing is performed by the Molecular Diagnostic Laboratory at Lurie Children's to detect mutations associated with Congenital Central Hypoventilation Syndrome-like symptoms.

The POTS Program at Lurie Children’s provides comprehensive care to patients with cardiovascular symptoms of Postural Orthostatic Tachycardia Syndrome (POTS). Learn more.

A group of rare syndromes that result from mutations in the PTEN gene, a gene that normally stops cells from growing and dividing uncontrolled (“suppressor genes”).

Lurie Children's Pediatric Palliative Care team focuses on improving the quality of life for children and their families.

An awareness of heartbeats, an uncomfortable but common complaint. A doctor can help determine if the palpitations are dangerous.

A condition affecting the growth plate at the end of the upper arm bone, in which it loses its blood supply and the nearby bone softens and collapses.

Sleep disorders among children are common. Issues that disrupt sleep once it has started, such as sleepwalking and night terrors, are known as “parasomnias.”

When the four pea-sized nodules located on or near the back of the thyroid gland are either overactive or underactive, releasing too much or too little parathyroid hormone.

A group of symptoms usually including tremor, slowness of movement, rigidity, and postural instability, similar to Parkinson's disease, but resulting from several causes.

A genetic defect causing the undifferentiated genitals of the developing baby to fail to respond correctly to male sex hormones, and not develop fully male characteristics.