Heath

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Cardiovascular diseases could be among the world’s first medical conditions to be treated by changing a patient’s genes. If ongoing phase 3 trials succeed, gene editing will offer a novel therapy for transthyretin amyloidosis, and treatments for hyperlipidemia may not be far behind.  Precise gene editing using clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein

Enough time had passed since the patient’s previous colonoscopy that she met the criteria to undergo another, said Steven Itzkowitz, a gastroenterologist at the Icahn School of Medicine at Mount Sinai in New York. She was in “reasonably good health,” and the risks of the procedure — bleeding, reaction to anesthesia, perforation of her colon

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