www.sciencedaily.com
Researchers have identified a rare, new form of diabetes affecting infants, caused by mutations in a single gene. These genetic changes impair the function of insulin-producing cells, leading to high blood sugar and the onset of diabetes. The condition is frequently associated with neurological complications. This discovery resolves a long-standing medical mystery, offering crucial insights into the broader mechanisms of diabetes and potentially guiding future treatments for genetic metabolic disorders.
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