What Is Friedreich’s Ataxia? Friedreich’s ataxia (FA) is a rare condition. It causes damage to your nervous system that gets worse over time. As a result, you may have abnormal movements ...

About DT-216P2 DT-216P2 is an improved formulation of a GeneTAC ® small molecule designed to specifically target the GAA repeat expansion mutation that is the underlying cause of FA and restore the ...

Billionaire Graeme Hart's granddaughter Jemima Hawkesby and her friend Flynn Mitchell graduating. She is fundraising to help ...

Broad Institute researchers have developed a way to edit the genetic sequences at the root of Huntington's disease and ...

Video content above is prompted by the following: Could you elaborate on the differential diagnosis for this disease, how it is definitively diagnosed and the impact of receiving such a diagnosis ...

SINCE Friedreich's original description 1 of 6 cases of familial hereditary ataxia in 1863, numerous papers have been written on this subject. The vast majority of these elaborate on the ...

to treat Friedreich's ataxia in individuals aged 16 years and above. This approval was granted through a national procedure. Friedreich's ataxia is a widespread hereditary ataxia type, affecting a ...

Nomlabofusp For The Treatment Of Patients With Friedreich's Ataxia As I stated above, the company released positive initial data from the long-term open-label extension [OLE] study, using ...

Larimar Therapeutics' CTI-1601, a potential first-in-class treatment for Friedreich's ataxia, shows promise in modifying disease progression and restoring mitochondrial function. The company has a ...

There are many types, including cerebellar ataxia, sensory ataxia, vestibular ataxia, Friedreich’s ataxia and more general forms of hereditary ataxias. The most common symptoms of the disease ...

Friedreich’s ataxia (FA) is a neurodegenerative disease most people have never heard of, and it remains widely misunderstood —and for the hundreds of Canadians who live with it, the lack of ...

Friedreich’s ataxia is a progressive neuromuscular disease that causes uncoordinated movement, muscle weakness, balance problems, impaired speech, and frequently, heart abnormalities.