Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Alternating Hemiplegia of Childhood in Korea: a Case Report.

Journal of Korean medical science - 6 Jul 2020

Shin Chaewon, Yoo Dallah, Kim Han Joon, Jeon Beomseok

Abstract excerpt

Alternating hemiplegia of childhood (AHC) is a rare neurodevelopmental disorder characterized by recurrent paroxysmal hemiplegic attacks that affect one or the other side of the body. Up to 74% of patients with AHC have a pathologic variant in the ATP1A3 gene. After the introduction of next-generation sequencing, intermediate cases and atypical cases have expanded the clinical spectrum of ATP1A3-related...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Brain
Share to Hemiplegia
Share to Heterozygote

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Magnetic Resonance Imaging

Share to Polymorphism, Single Nucleotide

Share to Republic of Korea

Share to Sodium-Potassium-Exchanging ATPase

Share to Whole Genome Sequencing

Source

Open in PubMed Open full text

Identifiers

PMID: 32627437
DOI: 10.3346/jkms.2020.35.e203
PMCID: PMC7338211

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Alternating Hemiplegia of Childhood in Korea: a Case Report.PMID 32627437Read ↗

Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review.Semantic proximity Read ↗

De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis.Semantic proximity Read ↗

Alternating Hemiplegia of Childhood Caused by ATP1A3 Mutations: A Report of Two Cases.Semantic proximity Read ↗

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.Semantic proximity Read ↗

Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients.Semantic proximity Read ↗

Alternating hemiplegia of childhood.Semantic proximity Read ↗

Alternating hemiplegia of childhood.Semantic proximity Read ↗

Alternating hemiplegia of childhood in Denmark: clinical manifestations and ATP1A3 mutation status.Semantic proximity Read ↗

Alternating Hemiplegia of Childhood: Genotype–Phenotype Correlations in a Cohort of 39 Italian PatientsSemantic proximity Read ↗

Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability.Semantic proximity Read ↗

Genotype–phenotype correlations in alternating hemiplegia of childhoodSemantic proximity Read ↗

Long-term follow up of an adult with alternating hemiplegia of childhood and a p.Gly755Ser mutation in the ATP1A3 gene.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.