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Article

Congenital mirror movements in a family: Outcomes associated with DCC mutations.

Journal of neurogenetics - 1 Jan 2025

Yücel Şen Arife Derda, Carman Kursat Bora, Doğan Çağrı, Şen Mustafa, Yarar Coşkun

Abstract excerpt

INTRODUCTION: Congenital mirror movement disorder refers to involuntary movements on one side of the body that mimic the deliberate movements on the opposite side. Congenital mirror movement is primarily associated with mutations in the DCC netrin-1 receptor (DCC) gene. CASE PRESENTATION: A 3-year-old child had been involuntarily grasping with one hand and then the other from infancy. His neuromotor development...

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Source

Identifiers

PMID: 40619166
DOI: 10.1080/01677063.2025.2525868

Genes

DCC

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Related research

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Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.Semantic proximity Read ↗

Identification of a homozygous splice site mutation in the dynein axonemal light chain 4 gene on 22q13.1 in a large consanguineous family from Pakistan with congenital mirror movement disorder.Semantic proximity Read ↗

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