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Getting to Know the Rare Neurological Condition, Movement Mirror Disorder

Getting to Know the Rare Neurological Condition, Movement Mirror Disorder
Illustration of movement mirror disorder. Credits: Freepik

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Movement Mirror Disorder (MMD) is a rare condition that disrupts the body’s motor coordination. Though uncommon, this disorder can significantly impact a person’s ability to perform everyday tasks that require distinct and controlled movements on each side of the body.

 

What is Movement Mirror Disorder?

Movement Mirror Disorder (MMD) is an unusual neurological condition in which involuntary movements occur on one side of the body when the other side is consciously moving. For instance, when you move your right hand, your left hand may move uncontrollably as well.

MMD is typically a congenital condition, present from birth, and is also referred to as Congenital Mirror Movement Disorder (CMMD). However, this disorder can persist into adulthood.

While MMD does not always result in significant disability, it can interfere with daily activities, particularly those requiring precise hand coordination, such as writing, playing musical instruments, exercising, or any tasks that demand fine motor skills.

 

Causes of Movement Mirror Disorder

Experts suggest that most cases of MMD and CMMD are inherited in an autosomal dominant pattern, meaning that an individual only needs to inherit one copy of the mutated gene from a parent to develop the condition.

Certain genes linked to CMMD, such as RAD51 and DNM2, are involved in the development of motor neuron pathways during fetal development. When mutations occur in these genes, the connections between the right and left hemispheres of the brain become abnormal, potentially disrupting motor control on both sides of the body.

Other research proposes that CMMD could stem from a failure in the differentiation of the corticospinal pathway during fetal growth. This pathway is responsible for controlling movements separately between the left and right sides of the body. Due to excessive connections in the motor pathways between both hemispheres, movements intended for one side can be reflected on the other.

Additionally, studies indicate that heightened activity in the primary motor cortex contributes to the development of MMD. While this condition is most commonly observed in the hands and arms, some individuals may also experience it in their legs.

 

How is Mirror Movement Disorder Treated?

MMD symptoms are often more pronounced during childhood but may lessen with age. If a child experiences frequent mirror movements or struggles with activities that require coordinated hand movement, it's important to seek a professional evaluation.

Pediatricians typically refer children to a neurologist for a comprehensive assessment. The examination process may include:

  • Observation of fine motor activities.

  • Electrophysiology tests.

  • MRI scans to detect any structural brain changes that could be linked to the condition.

  • Genetic tests to identify mutations in genes associated with CMMD.

Although there is no definitive cure for MMD, doctors typically recommend various therapies to help manage symptoms. Potential therapies include:

  • Physical and Occupational Therapy: To enhance coordination and muscle strength.

  • Motor Training: To develop fine and gross motor skills and improve movement control.

  • Medication: To support motor nerve function and alleviate symptoms.

  • Psychological Therapy: To assist children and their families in coping with the emotional effects of the disorder.

 

Though MMD is a complex condition that can affect the quality of life for individuals, with proper management through therapy, medication, and emotional support, those affected can still lead fulfilling lives.

It is crucial to consult a doctor if any symptoms appear. For convenience, you can also access medical consultations through the Ai Care app, available for download on the App Store or Play Store.

 

Looking for more information about other diseases? Click here!

 

Writer : Agatha Writer
Editor :
  • dr Hanifa Rahma
Last Updated : Sunday, 11 May 2025 | 21:41

Sabrina Schlienger, et all (2023). Genetics of mirror movements identifies a multifunctional complex required for Netrin-1 guidance and lateralization of motor control. Available from: https://pmc.ncbi.nlm.nih.gov/articles/PMC10181192 

Meagan L. Collins Hutchinson, MSc, et all (2024). Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals. Available from: https://movementdisorders.onlinelibrary.wiley.com/doi/10.1002/mds.29669 

Medline Plus (2015). Congenital mirror movement disorder. Available from: https://medlineplus.gov/genetics/condition/congenital-mirror-movement-disorder/#causes