In 2016 he donated €6,000 to bring Daire Flanagan, who was diagnosed with Apert Syndrome at birth, to an Everton game. Daire’s family wrote on their son’s gofundme page at the time: ...

Little Aaliya was born with an oddly shaped skull, no fingers and fused toes – clear signs of Apert’s syndrome, an incurable genetic disorder which affects one in 65,000 babies. “You know ...

Cushing syndrome occurs due to abnormally high levels of cortisol, which is commonly related to steroid use. Symptoms include weight gain, thinning skin, fluid retention, and stretch marks ...

But for a small number of children, the infection triggers strange behavioral changes known as PANDAS syndrome. PANDAS stands for pediatric autoimmune neuropsychiatric disorders associated with ...

Chronic fatigue syndrome — also known as myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) OR systemic exertional intolerance disease (SEID)— is a serious, chronic illness that can ...

The purpose of a systematic physical assessment in the newborn period is to examine for any anomalies, establish a baseline for observations and comparisons, and initiate referrals for continued ...

Cleft lip and cleft palate (CL/CP) are the most commonly occurring craniofacial birth defects. Although some CL/CPs are detected on prenatal ultrasound, the majority are immediately recognized in ...

Klinefelter syndrome is a genetic condition that affects only males. Here's what you should know about the causes, symptoms, and treatment options for the condition. Klinefelter syndrome is a genetic ...

What is Guillain-Barré syndrome? Guillain-Barré syndrome (GBS) is also called acute inflammatory demyelinating polyradiculoneuropathy (AIDP). It's a neurological disorder in which the body's immune ...