Ryan Becker from Spokane is battling a rare medical condition that has left doctors at the Mayo Clinic and Johns Hopkins ...
A Dublin girl born with the most severe form of butterfly skin is excited as she prepares to go to secondary ... move from primary to secondary school later this year. Ahead of Rare Disease Day on ...
Years ago, a family member was diagnosed with an extremely rare cancer: Liposarcoma of the Spermatic Cord. Fewer than 200 ...
STATEN ISLAND, N.Y. — A fundraising Polar Plunge to honor John Hudson Dilgen will take place this month in South Beach to ...
Seventeen-year-old Hamzah has congenital ichthyosis, a disorder that causes hard, scaly skin. It also affects his vision, ...
The proprietary Invisicare delivery technology has exclusive rights for all orphan rare skin disease applications, enhancing Quoin's competitive advantage in the pharmaceutical market. The company ...
said the hospital has established a hereditary skin disease clinic to ensure the availability of long-term treatment for patients, including "butterfly children" and other rare disease sufferers.
Despite multiple treatments for eczema and pityriasis alba, a child’s skin condition worsened until a biopsy revealed mycosis fungoides.
ASHBURN, Va., March 04, 2025 (GLOBE NEWSWIRE) -- Quoin Pharmaceuticals Ltd. (NASDAQ: QNRX) (the “Company” or “Quoin”), a late clinical stage, specialty ...
A Dublin girl born with the most severe form of butterfly skin is excited as she prepares ... to secondary school later this year. Ahead of Rare Disease Day on Friday, Debra, the national charity ...