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Congenital Mirror Movements in A Family with TUBB2B Mutation
Suhani Shah1, Anaita Udwadia Hegde1, Kavya Rajarajan1
1SRCC Children's Hospital managed by Narayana Health, Mumbai, India.
Movement Disorders Clinical Practice
|October 6, 2025
Summary
Congenital mirror movements (CMM) are involuntary mirroring movements. This study links TUBB2B gene mutations to CMM, expanding the understanding of its genetic causes and neuronal migration roles.
Area of Science:
- Neuroscience
- Genetics
- Developmental Biology
Background:
- Congenital mirror movements (CMM) involve involuntary mirroring of movements between body sides.
- While several genes are linked to CMM, tubulinopathies like TUBB3 mutations are emerging as potential contributors.
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