Familial congenital mirror movements

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ORPHA:238722OMIM:618264G25.8
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2Specialists8Treatment centers

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Overview

Familial congenital mirror movements (also known as congenital mirror movements or bimanual synkinesis) is a rare neurological condition characterized by involuntary movements of one side of the body that mirror intentional movements made on the opposite side. These mirror movements predominantly affect the hands and fingers, meaning that when a person performs a voluntary movement with one hand, the other hand simultaneously and involuntarily performs the same movement. The condition is present from birth or early infancy and typically persists throughout life, though the severity of mirror movements may slightly decrease with age in some individuals. The underlying cause involves abnormal development of the corticospinal tract, the major nerve pathway that connects the brain to the spinal cord and controls voluntary movement. In healthy individuals, the corticospinal tract is predominantly crossed (contralateral), meaning each hemisphere of the brain controls the opposite side of the body. In familial congenital mirror movements, there is an abnormal ipsilateral (same-side) corticospinal projection, resulting in both hemispheres simultaneously activating muscles on both sides. Mutations in the DCC (deleted in colorectal carcinoma) gene on chromosome 18q21.2 and the RAD51 gene on chromosome 15q15.1 have been identified as causes. The DCC gene encodes a receptor involved in axon guidance, particularly in the midline crossing of corticospinal tract fibers. The condition primarily affects the motor system, and individuals generally have normal muscle strength, coordination, and cognitive function. However, mirror movements can cause significant functional impairment in daily activities requiring independent bimanual hand movements, such as typing, playing musical instruments, or performing fine motor tasks. There is currently no curative treatment for familial congenital mirror movements. Management is supportive and may include occupational therapy to help individuals develop compensatory strategies for tasks requiring independent hand use. The condition does not typically worsen over time and is not associated with other neurological deterioration.

Also known as:

Clinical phenotype terms— hover any for plain English:

Bimanual synkinesiaHP:0001335Abnormal corticospinal tract morphologyHP:0002492Easy fatigabilityHP:0003388Dysgenesis of the hippocampusHP:0025101Fused cervical vertebraeHP:0002949
Inheritance

Autosomal dominant

Passed on from just one parent; each child has about a 50% chance of inheriting it

Age of Onset

Neonatal

Begins at or shortly after birth (first 4 weeks)

Orphanet ↗OMIM ↗NORD ↗

Treatments

No FDA-approved treatments are currently listed for Familial congenital mirror movements.

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No actively recruiting trials found for Familial congenital mirror movements at this time.

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Specialists

2 foundView all specialists →
RP
Rocío Palomo, Physiotherapist
Specialist
PI on 1 active trial

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Familial congenital mirror movements.

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Community

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Common questions about Familial congenital mirror movements

What is Familial congenital mirror movements?

Familial congenital mirror movements (also known as congenital mirror movements or bimanual synkinesis) is a rare neurological condition characterized by involuntary movements of one side of the body that mirror intentional movements made on the opposite side. These mirror movements predominantly affect the hands and fingers, meaning that when a person performs a voluntary movement with one hand, the other hand simultaneously and involuntarily performs the same movement. The condition is present from birth or early infancy and typically persists throughout life, though the severity of mirror m

How is Familial congenital mirror movements inherited?

Familial congenital mirror movements follows a autosomal dominant inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.

At what age does Familial congenital mirror movements typically begin?

Typical onset of Familial congenital mirror movements is neonatal. Age of onset can vary across affected individuals.

Which specialists treat Familial congenital mirror movements?

2 specialists and care centers treating Familial congenital mirror movements are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.