Familial congenital mirror movements

Orpha code: 238722OMIM code: 616059

Definition

A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities.

Disease data
Classification

Disease

Synonyms
Familial congenital controlateral synkinesia
Dziedziczna wrodzona synkinezja kontrlateralna
Dziedziczne wrodzone ruchy lustrzane
Izolowana wrodzona synkinezja kontrlateralna
Izolowane wrodzone ruchy lustrzane
Rodzinna wrodzona synkinezja kontrlateralna
Hereditary congenital controlateral synkinesia
Hereditary congenital mirror movements
Isolated congenital controlateral synkinesia
Isolated congenital mirror movements
ORPHA code
238722
OMIM code
616059
ICD10 code
G25.8
ICD11 code
-

No additional description.

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