An 84-year-old man left clinicians at a Hong Kong hospital utterly perplexed after arriving at the hospital to be treated […] ...
Argyria is caused by a buildup of silver in the body, which discolors the skin.
Managing the unpredictable symptoms of indolent systemic mastocytosis prompted a search for answers and community.
Epidermolysis Bullosa (EB), or butterfly disease, affects 1 in 50,000 people, causing fragile skin that blisters easily, ...
Work It’s Hui Wong speaks to Dr Mark Koh, Leading Dermatologist at Rare Skin Conditions Society of Singapore (RSC), on their ...
Researchers find that allergy medicine could help patients with a rare genetic disease avoid liver transplants.
Sanofi and Regeneron's Dupixent has become the first biologic drug to show activity in prurigo nodularis (PN), raising the hope of a new treatment option for the rare and highly debilitating skin ...
A common antihistamine may offer hope for patients with a rare genetic disease that can lead to severe liver damage and ...
Arctic therapeutics raises funding from EIC Fund, Kaldbakur, and Sanos Group to advance its dementia treatment, AT-001, and acne drug, AT-004. The company aims to transform the treatment landscape for ...
Skinvisible granted Quoin an exclusive, royalty-bearing license to its technology for use in select rare skin diseases and for the right to use its proprietary formula for Netherton Syndrome.