Genomenon, a leader in genomic intelligence, today announced a strategic partnership with UCB to accelerate awareness, diagnosis, and research for thymidine kinase 2 deficiency (TK2d).

The inheritance pattern of this disorder varies among these breeds. Typically, it is inherited in either an autosomal recessive or autosomal dominant manner, although the recessive form is more common ...

Nectarines: There is a common misconception that nectarines are a cross between a plum and a peach, but that’s not at all the ...

One-time surgical application of genetically engineered autologous keratinocyte sheets provides significant closure and pain ...

The study also included older children and found the best outcomes in patients between 5 years and 8 years old.

A new gene therapy has shown promising results in restoring hearing to children, teens, and even a young adult born with a ...

CLEVELAND, July 02, 2025 (GLOBE NEWSWIRE) -- Abeona Therapeutics Inc. (Nasdaq: ABEO) today announced the closing of the sale of its Rare Pediatric Disease Priority Review Voucher (PRV) for gross ...

Gene therapy can improve hearing in children and adults with congenital deafness or severe hearing impairment, a new study ...

A rare albino deer was recently spotted in our viewing area, and ABC13 reached out to wildlife experts to ask some questions ...

Werewolf Cat's Reaction to Eating French Fries Is All of Us in the McDonald's Drive Thru originally appeared on PetHelpful. I ...

For patients with recessive dystrophic epidermolysis bullosa (RDEB), a one-time surgical application of prademagene ...

Panelists discuss how spinal muscular atrophy is an autosomal recessive genetic disease affecting motor neurons with 3 ...