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Article

Congenital Mirror Movements in A Family with TUBB2B Mutation.

Movement disorders clinical practice - 1 Mar 2026

Shah Suhani, Hegde Anaita Udwadia, Rajarajan Kavya, Panwala Hiren

Abstract excerpt

BACKGROUND: Congenital mirror movements (CMM) are involuntary movements on one side of the body that mirror intentional movements on the opposite side, which persist in adult life. While mutations in DCC, RAD51, NTN1 and other genes have been associated with CMM, recent evidence suggests tubulinopathies, including TUBB3 mutations, may also contribute. CASES: An 11-year-old girl with developmental delay and CMM...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 41048055
DOI: 10.1002/mdc3.70385
PMCID: PMC13042980

Genes

TUBB2B
DCC
NTN1
RAD51
TUBB3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Congenital Mirror Movements in A Family with TUBB2B Mutation.PMID 41048055Read ↗

An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation.Semantic proximity Read ↗

Mirror movements and callosal dysgenesis in a family with a DCC mutation: Neuropsychological and neuroimaging outcomes.Semantic proximity Read ↗

De novo TUBB2B mutation causes fetal akinesia deformation sequence with microlissencephaly: An unusual presentation of tubulinopathy.Semantic proximity Read ↗

Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development.Semantic proximity Read ↗

TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy.Semantic proximity Read ↗

Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected IndividualsSemantic proximity Read ↗

Congenital mirror movements in a family: Outcomes associated with DCC mutations.Semantic proximity Read ↗

Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene.Semantic proximity Read ↗

RAD51 haploinsufficiency causes congenital mirror movements in humans.Semantic proximity Read ↗

Overlapping cortical malformations and mutations in TUBB2B and TUBA1A.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 ↗

The spectrum of brainstem malformations associated to mutations of the tubulin genes family: MRI and DTI analysis.Semantic proximity Read ↗

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