Tribune News NetworkDohaSidra Medicine, a member of Qatar Foundation, has established a Gene Therapy Center to treat rare genetic diseases such as Spinal Muscular Atrophy (SMA) and Duchenne Muscular ...
The 18-year-old's mom and sister work hard to give her the life she deserves as she battles a rare genetic condition ...
Sidra Medicine, a member of Qatar Foundation, has established a gene therapy centre to treat rare genetic diseases such as ...
Seattle doctors developed a blood test that determines the parental origin of the RB1 mutation in retinoblastoma.
The early stage company is developing a new approach to gene editing to treat rare genetic diseases. It does this using mRNA, ...
Advances in genetic testing, enable the identification of genetic causes even before symptoms appear, allowing for timely ...
Joshua Mercieca defied the odds after he was diagnosed with the muscle-wasting condition Duchenne muscular dystrophy at a ...
Marcelo was diagnosed with Treacher Collins syndrome, a rare condition affecting facial bone structure and cartilage. The ...
Nikita Naiyar, a child artist and daughter of media professional Namitha Madhavankutty, passed away on Sunday, January 26 ...
Pioglitazone was associated with a lower risk of developing skin ulcers in patients with Werner disease in a Japanese study, ...
Wiskott-Aldrich syndrome is a rare genetic immunodeficiency that keeps a child's immune system from functioning properly. It ...