Doctors confirm rare gene mutation in child which causes changes in how immune system behaves during early development ...

A study led by the Research Institute of the McGill University Health Center (The Institute) has identified a rare genetic ...

The Nairobi West Hospital successfully repaired a complex heart defect in a 40 year old woman, highlighting gaps and growing ...

Dr. Jennifer Adams, whose daughter was diagnosed at 18 months with PH1, calls Oxlumo a "life-changing medication." As a result, her daughter's "quality of life has improved, hospital visits were ...

A team of Indian researchers has identified a rare USP18 gene mutation linked to recurrent neurological decline in children.

New videos of interstellar comet 3I ATLAS have ignited public interest. Online discussions suggest the comet might be ...

Earlier this week, cruise line stocks including Norwegian Cruise Line Holdings, Royal Caribbean, and Carnival Corporation experienced a sudden and broad decline, with the trigger for this pullback not ...

Harvard astrophysicist Dr Avi Loeb tells ABP Live that 3I/ATLAS shows several odd behaviours, from unusual jets to rare ...

Published research expands clinical understanding of Pseudo-TORCH syndrome type 2 through discovery of an unreported variant ...

Redcliffe Labs reports a groundbreaking discovery of a novel USP18 gene mutation associated with a rare neurological disorder in children, offering new insights into unprecedented cases of ...

Tom Cruise, a devoted father, navigates his relationships with children Isabella, Connor, and Suri amidst complex circumstances. Shaped by a difficult ...