Researchers from Radboud University Medical Center and University of Basel have discovered new genetic causes of inherited ...

Sickle cell anemia is the world's most common genetic disorder. It causes the red blood pigment hemoglobin to crystallize, ...

A new University of California San Diego School of Medicine study offers a unified biological model to explain how genetic predispositions and environmental exposures converge to cause autism spectrum ...

Rare genetic disorders affect more than 300 million people worldwide, with children making up 70% of those impacted, according to EURORDIS. These conditions often go undiagnosed for years due to ...

Becky Quick opens up about her 9-year-old daughter Kaylie’s rare genetic disorder, explaining the symptoms, diagnosis, and ...

Neonatal adrenoleukodystrophy (NALD) is the former name of a rare genetic disorder known as Zellweger spectrum disorder (ZSD). Doctors usually diagnose it shortly after birth, and treatment includes ...

PKD is mainly caused by mutations in the PKD1 and PKD2 genes, affecting polycystin proteins. Disrupted signaling pathways, like cAMP and vasopressin, are major drivers of cyst growth. Tolvaptan is ...

Recent studies have uncovered intriguing details about Adolf Hitler’s personal biology. The infamous Nazi leader, responsible for horrific crimes during World War Two, is believed to have had a rare ...

SOUTH SAN FRANCISCO, Calif., June 05, 2024 (GLOBE NEWSWIRE) -- 23andMe Holding Co. (ME), a leading human genetics and biopharmaceutical company, today released a new genetic Bipolar Disorder report ...

"GMA3" spoke to the Lemay-Pelletier family about their incredible journey. A family of six spent the last year traveling the world together to take in as many sights as possible before retinitis ...