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Results 1 - 9 of 9 for Mirror movements 1
  1. Congenital mirror movement disorder 
    ... Isolated congenital controlateral synkinesia Isolated congenital mirror movements Mirror movements 1 Genetic Testing Registry: Mirror movements 1 Familial congenital ...
    https://medlineplus.gov/.../congenital-mirror-movement-disorder - Genetics
  2. NTN1 gene 
    ... Mutations in the netrin-1 gene cause congenital mirror movements. J Clin Invest. 2017 Nov 1;127(11):3923-3936. doi: 10.1172/JCI95442. ...
    https://medlineplus.gov/genetics/gene/ntn1 - Genetics
  3. DCC gene 
    ... control in the human nervous system: genetics of mirror movements. Curr Opin Neurobiol. 2013 Feb;23(1):109-18. doi: 10.1016/j.conb.2012. ... F, Rouleau GA. Mutations in DCC cause congenital mirror movements. Science. 2010 Apr 30;328(5978):592. doi: 10.1126/science.1186463. Citation on PubMed
    https://medlineplus.gov/genetics/gene/dcc - Genetics
  4. RAD51 gene 
    ... CL, Robertson SP, Gardner RJM, Markie D. Congenital mirror movements: phenotypes associated with DCC and RAD51 mutations. J Neurol Sci. 2015 Apr 15;351(1-2):140-145. doi: 10.1016/j.jns. ...
    https://medlineplus.gov/genetics/gene/rad51 - Genetics
  5. ANOS1 gene 
    ... to develop (unilateral renal agenesis), hearing loss, and mirror movements of the hands (bimanual synkinesia). Because these features vary among individuals, researchers suspect that other genetic and environmental factors ... adhesion molecule-like X-linked ADMLX anosmin-1 HHA KAL KAL1 KALIG-1 Kallmann syndrome 1 ...
    https://medlineplus.gov/genetics/gene/anos1 - Genetics
  6. 7q11.23 duplication syndrome 
    ... movements of one side of the body that mirror intentional movements of the other side. About one-fifth of ...
    https://medlineplus.gov/.../condition/7q1123-duplication-syndrome - Genetics
  7. Primary ciliary dyskinesia 
    ... the brain. Primary ciliary ... for cilia to bend. Coordinated back and forth movement of cilia is necessary for the normal functioning ...
    https://medlineplus.gov/.../condition/primary-ciliary-dyskinesia - Genetics
  8. POLG gene 
    ... is characterized by seizures, loss of mental and movement abilities (psychomotor regression), and liver disease. The liver ... This condition weakens the muscles that control eye movement and causes the eyelids to droop (ptosis).There ...
    https://medlineplus.gov/genetics/gene/polg - Genetics
  9. PITX1 gene 
    ... regulatory elements. Dev Biol. 2013 Feb 1;374(1):234-44. doi: ... malformations including mirror-image polydactyly. Eur J Hum Genet. 2012 Jun; ...
    https://medlineplus.gov/genetics/gene/pitx1 - Genetics