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Familial congenital mirror movements

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Name:
Familial congenital mirror movements
Description:
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.
ORPHAcode:
238722
Synonyms:
Familial congenital controlateral synkinesia
Hereditary congenital controlateral synkinesia
Hereditary congenital mirror movements
Isolated congenital controlateral synkinesia
Isolated congenital mirror movements
XREF(s):
Orphanet
OMIM
OMIM
OMIM
OMIM
ICD-10
Analyte(s):
DNAL4
RAD51
DCC
NTN1
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14