ATP1A3-Related Relapsing Encephalopathy with Cerebellar Ataxia (RECA): A Genetic Disorder with an Inflammatory Basis?

Martin, Andrew J; Ong, Tien-Lee; Briceno-Morales, Hugo; Tchan, Michel; Fung, Victor S C

Martin, Andrew J; Ong, Tien-Lee; Briceno-Morales, Hugo; Tchan, Michel; Fung, Victor S C.

Afiliación

Martin AJ; Movement Disorders Unit, Neurology Department, Westmead Hospital Westmead New South Wales Australia.
Ong TL; Blacktown Hospital Blacktown New South Wales Australia.
Briceno-Morales H; Movement Disorders Unit, Neurology Department, Westmead Hospital Westmead New South Wales Australia.
Tchan M; Hospital Sultanah Nur Zahirah, Department of Medicine Kuala Terengganu Malaysia.
Fung VSC; Movement Disorders Unit, Neurology Department, Westmead Hospital Westmead New South Wales Australia.

Mov Disord Clin Pract ; 9(8): 1120-1123, 2022 Nov.

Article en En | MEDLINE | ID: mdl-36339296

Palabras clave

ATP1A3; CAPOS; RECA; alternating hemiplegia of childhood; antiGAD; neopterin; rapidonset dystonia parkinsonism; relapsing encephalopathy with cerebellar ataxia

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