An 84-year-old man left clinicians at a Hong Kong hospital utterly perplexed after arriving at the hospital to be treated […] ...
Jeremiah Marshall has lived with epidermolysis bullosa since the day he was born and has had to endure teasing at school, ...
Mayo Clinic's organoids, microscopic versions of organs that function like the real ones, have been used by doctors to study ...
A MUM suffering severe bloating died after she had a suspected allergic reaction to a CT scan. Yvonne Graham, 66, went into ...
In two new papers, researchers from The Jackson Laboratory (JAX) report the successful use of two approaches—gene therapy and ...
Jeremiah Marshall, 33, has epidermolysis bullosa, a rare genetic disorder that makes his skin tear or blister at the ...
An editor in his early 40s thought the tiny numb spot on his nose was innocuous. A year and six doctors later, he learned it ...
For the first time since 2018, the Navesink River was frozen enough for ice boaters to take their crafts out on the solid ...
Calls have been made for specific guidelines for the public health response to patients with leprosy after a recent case ...
Timber's lead candidate TMB-001 for rare skin disease congenital ichthyosis failed to meet its efficacy objectives across the board in the ASCEND trial and will not support a planned regulatory ...
German drugmaker Boehringer Ingelheim has its first regulatory approval for spesolimab, its antibody therapy for rare and life-threatening ... treat other skin diseases, such as palmoplantar ...