They applied this technique from a common disease to rare diseases. Their research could pave the way for a new and effective ...
Carter Bresee was born with lamellar ichthyosis (LI) a rare genetic skin disorder in which the body creates skin cells that ...
A man living with a rare condition that causes half of his face to shrink has shared the 'hardest part' about dealing with it ...
Newser on MSN3d
Biologist With Rare Rapid-Aging Disease Dies at 28Italian molecular biologist Sammy Basso has died at age 28—almost double the typical life expectancy for someone with the ...
A local clinic specializing in the treatment of fibromyalgia and Ehlers-Danlos syndrome (EDS) is closing, leaving patients ...
What Is Thrombocytopenic Purpura: Rare Disease that Has Plagued Julia Roberts for Almost Two Decades
Despite battling a rare blood disorder for years, Julia Roberts continues to captivate audiences with her iconic performances ...
2don MSNIn Depth
Emma Fogarty, who lives with epidermolysis bullosa, or EB, have been friends for 16 years after meeting at a charity event.
That was a modest wager on a drug that stood a chance of becoming the first FDA-approved topical therapy for congenital ichthyosis, a collection of around 20 rare skin disorders that cause dry ...
Irish Independent on MSN4d
Colin Farrell’s Dublin marathon bid raises thousands for friend with rare skin disorderColin Farrell has thanked the public for backing his charity marathon run for a friend with an agonising skin condition after ...
The website you are visiting is protected and accelerated by Incapsula. Your computer may have been infected by malware and ...
Sam Gallo is the founder of the Louisiana Diabetes Association and the man responsible for centralizing research and data for ...
Carter, the 7-year-old boy with a rare skin condition is finally able to rest his eyes after his life changing surgery in San Diego.
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback