Expanding Phenotype of ATP1A3 - Related Disorders: A Case Series.
Child Neurol Open
; 8: 2329048X211048068, 2021.
Article
en En
| MEDLINE
| ID: mdl-34761051
ABSTRACT
Neurologic disorders caused by mutations in the ATP1A3 gene were originally reported as three distinct rare clinical syndromes Alternating Hemiplegia of Childhood (AHC), Rapid-onset Dystonia Parkinsonism (RDP) and Cerebellar ataxia, Areflexia, Pes cavus, Opticus atrophy and Sensorineural hearing loss (CAPOS). In this case series, we describe 3 patients. A mother and her daughter showed an intermediate phenotype different from each other with the same heterozygous missense mutation (p.[R756C]), recently described in literature as Relapsing Encephalopathy With Cerebellar Ataxia (RECA). In addition, a third patient showed an intermediate AHC-RDP phenotype and had a likely pathogenic novel de novo missense mutation (p.[L100â
V]). These patients support the growing evidence that AHC, RDP and RECA are part of a continuous ATP1A3 mutation spectrum that is still expanding. Three common features were a sudden onset, asymmetrical neurological symptoms, as well as the presence of triggering factors. When present, the authors argue to perform exome sequencing in an early stage.
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1
Colección:
01-internacional
Base de datos:
MEDLINE
Idioma:
En
Revista:
Child Neurol Open
Año:
2021
Tipo del documento:
Article
País de afiliación:
Países Bajos