Nino has a rare neurologic disorder called ATP1A3 syndrome which affects his mobility and means he is non-verbal. Eve said Nino loves "the feeling of being free because he's unable to walk.

Pathogenic variation in the ATP1A3‐encoded sodium‐potassium ATPase, ATP1A3, is responsible for alternating hemiplegia of childhood (AHC). Although these patients experience a high rate of sudden ...

Estella Henderson was born with a mutation on her ATP1A3 gene – a degenerative and very rare condition that leads to the disease alternating hemiplegia of childhood or AHC, which for Estella ...

A 5-year-old girl appeared to not let anything come between her and her preschool graduation – not even paralysis. Estella Henderson was born with a mutation on her ATP1A3 gene – a ...

Alternating Hemiplegia is a debilitating neurodevelopmental disorder that stems from a mutation in the ATP1A3 gene. This condition affects children at an early age and has a major impact on their ...

(Photo: Mary Saladino) AHC can be caused by 163 different mutations in the ATP1A3 gene, but three mutations, including the one that Henry has, account for 75% of cases, according to Swoboda.

AHC can be caused by 163 different mutations in the ATP1A3 gene, but three mutations, including the one that Henry has, account for 75% of cases, according to Swoboda. The ATP1A3 gene encodes a ...

Then imagine that these symptoms do not go away. That dramatic and often devastating experience is among the many ways that a group of disorders caused by a mutation in the ATP1A3 gene can affect ...

That dramatic and often devastating experience is among the many ways that a group of disorders caused by a mutation in the ATP1A3 gene can affect patients. Originally called rapid onset dystonia ...