Jul 16, 2025
Progeria, also known as Hutchinson-Gilford Progeria Syndrome (HGPS) and Benjamin button disease, is one of the rarest and most dramatic genetic disorders known to medicine. Characterized by rapid and premature ageing in children, this condition affects approximately 1 in 20 million people worldwide. Children with p...
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Discover How Learning Disability Treatment Landscape is Evolving with the Emergence of Digital Assistant Technologies
Jul 04, 2025
A New Era for Multiple Myeloma Treatment: Bispecific Antibodies Enter the Fray
Jun 10, 2025
LEQEMBI: A New Hope for Alzheimer’s Disease Patients
Feb 12, 2025
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