CONDITION REFERENCE
Congenital mirror movement disorder
Information from MedlinePlus Genetics about this condition and how it can be inherited.
About this condition
Congenital mirror movement disorder is a condition in which intentional movements of one side of the body are mirrored by involuntary movements of the other side. For example, when an affected individual makes a fist with the right hand, the left hand makes a similar movement. The mirror movements in people with this disorder primarily affect the arms, and the hands and fingers are always involved. This pattern of movements is present from infancy or early childhood and usually persists throughout a person's life.
People with congenital mirror movement disorder can have some difficulty with certain daily activities, particularly with those that require different movements in each hand, such as typing on a keyboard. They may experience discomfort or pain in their arms during prolonged use of the hands.
The extent of the mirror movements in people with congenital mirror movement disorder can vary, even within the same family. In most cases, the involuntary movements are noticeable but less pronounced than the corresponding voluntary movements. The extent of the movements typically stay the same throughout the lifetime of an affected individual.
In general, mirror movements are the only feature associated with this condition. In some cases, however, people with congenital mirror movement disorder can have partial or complete absence (agenesis) of the tissue that connects the left and right halves of the brain (corpus callosum).
Mirror movements can also occur in people who do not have congenital mirror movement disorder. Mild mirror movements are common during the normal development of young children, and they typically disappear before age 7. They can also develop later in life in people with neurodegenerative disorders such as Parkinson's disease. Mirror movements may also be present in people with certain conditions that have a wider range of signs and symptoms (syndromes).
Inheritance
- Autosomal recessive
- Autosomal dominant, inherited from one affected parent
A condition can have several forms with different inheritance patterns. Each pattern may apply to a different gene or form of the condition.
Related genes
MedlinePlus lists these genes for this condition. Open a gene page to read any available ClinGen reviews and ClinVar records.
YOUR DNA FILE
What can your DNA file tell you?
Your DNA file only includes the positions your test checked and reported. Consumer DNA kits usually test selected positions. Sequencing files can also leave out positions that were not reported or where the test could not give a result.
A variant missing from your file does not mean you tested negative for it. A ClinVar classification applies to a particular variant and the condition or finding it was reported for. It does not apply to everyone with that gene. An uncertain finding cannot establish a diagnosis.
BioDecode reads supported DNA files on your computer. It cannot fill gaps in your test, diagnose a condition or replace clinical testing.
Sources and dates
The source information on this page last changed on 2026-09-18.
MedlinePlus Source details
Source release: Fri, 18 Sep 2026 05:17:13 GMT
Source publication: 2025-05-19
Source review: 2025-05
SHA-256: fdc8bd614310c12718379cef6569962e5d0e791cecabcc355b53a72816ac263a
About the library sources · Latest validated release · Record de7b11445246