AT is inherited in an autosomal recessive manner, so to manifest the condition you must inherit an abnormal gene for the ATM ...

Some families call it as a test of faith, while others deem it a curse. Spinocerebellar ataxia 4 (SCA4), a rare but ...

Phase II data indicate Larimar Therapeutics’ injectable therapy nomlabofusp could go head-to-head in the market with Biogen's ...

Spinocerebellar ataxia 4 is a devastating progressive movement disease that can begin as early as the late teens. Now, a multinational research team has conclusively identified the genetic difference ...

A cluster of cats on a Texas dairy farm died after drinking raw milk from dairy cows affected with bird flu, according to a ...

New Evidence Indicates ATH434 can Function as an Iron Chaperone to Redistribute Iron –MELBOURNE, Australia and SAN FRANCISCO, April 29, ...

If you read my story “Finishing touches” about an exhibition showcasing Santa Fe artist Al Kittel’s work, you might be ...

Researchers have conclusively identified the genetic cause of a rare, progressive movement disorder. A rare extra-long ...

Lexeo on Tuesday said the designation covers LX2006 in the treatment of cardiomyopathy in patients with Friedreich's ataxia, an inherited disorder that causes progressive damage to the nervous system.

His friends’ teenage son and daughter were both diagnosed with Friedrich's ataxia. The family’s world was turned upside down ...

Kittel, 32, suffers from Friedreich's ataxia, a progressive neurological condition that saps abilities and energy and dramatically shortens lifespans. After watching her brother Aaron die of the same ...

LX2006 (AAVrh.10hFXN) is an adeno-associated virus gene therapy candidate designed to deliver a functional frataxin gene to cardiac cells to improve mitochondrial function. The Food and Drug ...