CAPOS Syndrome Latest Advances

Find the Latest Research About CAPOS Syndrome

Last Updated: 02/24/2026

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Found 48 publications

CAPOS and Beyond: ATP1A3 Variants in Pediatric Movement Disorders - Case Reports.

CAPOS and Beyond: ATP1A3 Variants in Pediatric Movement Disorders - Case Reports.

Journal: Molecular syndromology
Published: July 03, 2025

Clinical features of CAPOS syndrome caused by maternal ATP1A3 gene variation: a case report

Clinical features of CAPOS syndrome caused by maternal ATP1A3 gene variation: a case report

Journal: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery
Published: November 13, 2023

Childhood fever and hearing loss associated with CAPOS syndrome.

Childhood fever and hearing loss associated with CAPOS syndrome.

Journal: Auris, nasus, larynx
Published: September 29, 2023

Is meal order timing and flexibility key to improving patient satisfaction with hospital foodservice?

Is meal order timing and flexibility key to improving patient satisfaction with hospital foodservice?

Journal: Journal of human nutrition and dietetics : the official journal of the British Dietetic Association
Published: March 06, 2023

ATP1A3-related phenotypes in Chinese children: AHC, CAPOS, and RECA.

ATP1A3-related phenotypes in Chinese children: AHC, CAPOS, and RECA.

Journal: European journal of pediatrics
Published: April 08, 2022

A Rare Cause of Recurrent Febrile Encephalopathy in a Child: The Expanding Spectrum of ATP1A3 Mutations.

A Rare Cause of Recurrent Febrile Encephalopathy in a Child: The Expanding Spectrum of ATP1A3 Mutations.

Journal: Cureus
Published: December 13, 2021

Hemidystonia with polymicrogyria is part of ATP1A3-related disorders.

Hemidystonia with polymicrogyria is part of ATP1A3-related disorders.

Journal: Brain & development
Published: August 05, 2021

Auditory Neuropathy as the Initial Phenotype for Patients With ATP1A3 c.2452 G > A: Genotype-Phenotype Study and CI Management.

Auditory Neuropathy as the Initial Phenotype for Patients With ATP1A3 c.2452 G > A: Genotype-Phenotype Study and CI Management.

Journal: Frontiers in cell and developmental biology
Published: July 29, 2021

The diagnostic spectrum of ATP1A3-related disorders: 3 new patients.

The diagnostic spectrum of ATP1A3-related disorders: 3 new patients.

Journal: Journal of the neurological sciences
Published: June 15, 2021

Long-Term Follow-Up of a Patient with a De Novo p.Arg769Cys Mutation in the ATP1A3 Gene.

Long-Term Follow-Up of a Patient with a De Novo p.Arg769Cys Mutation in the ATP1A3 Gene.

Journal: Movement disorders clinical practice
Published: April 19, 2021

ATP1A3-Related Disorders: An Ever-Expanding Clinical Spectrum.

ATP1A3-Related Disorders: An Ever-Expanding Clinical Spectrum.

Journal: Frontiers in neurology
Published: December 04, 2020

An 88.8-kb Novel Deletion of 19q13.2 Encompassing the ATP1A3 Gene Detected by Array CGH in a Patient with Delayed Psychomotor Development, Generalized Hypotonia and Macrocephaly.

An 88.8-kb Novel Deletion of 19q13.2 Encompassing the ATP1A3 Gene Detected by Array CGH in a Patient with Delayed Psychomotor Development, Generalized Hypotonia and Macrocephaly.

Journal: Molecular syndromology
Published: November 07, 2020
Showing 1-12 of 48

Last Updated: 02/24/2026