A Delaware County infant with a rare metabolic disease, CPS1 deficiency, was treated at CHOP with a custom CRISPR therapy.

Prader-Willi syndrome is a rare genetic disease that causes poor feeding in infancy but later triggers insatiable hunger.

An infant with a rare urea cycle disorder became the first patient to receive a personalized gene-editing therapy. His care ...

KJ received the bespoke CRISPR treatment 6.5 months after birth, receiving three infusions of the therapy as of April 2025.

Dopamine deficiency occurs when levels of the neurotransmitter dopamine are low, affecting movement, emotions, sleep, and ...

The goal is to reuse key parts of the treatment and simply swap in a custom set of instructions for each patient's specific ...

You need a cure for your Trump derangement syndrome. Quitting smoking is easier than ending friendships with MAGA folks. Eventually you run out of friends. Always remember, if you change nothing ...

Iodine serves as the fundamental building block for thyroid hormones, and deficiency remains the leading ... athletes with relative energy deficiency syndrome. Certain medical treatments and ...

Many say they felt attacked by debilitating waves of sound and pressure known as "Havana syndrome." Sunday, 60 Minutes reported… U.S. defense official had ‘Havana syndrome’ symptoms during a ...

"We still have no definitive idea of the risks involved in pregnancy for women with chronic fatigue syndrome. The suggestion that it's okay to be pregnant is not yet substantiated by science.

aol.com Iron deficiency anaemia (IDA) occurs in 2–5% of adult men ... abdominal mass or cutaneous signs of rare causes of GI blood loss (eg, Peutz–Jeghers syndrome and hereditary haemorrhagic ...