Cerebral Palsy
Cerebral palsy: Public Health and Genomic Insights - August 4, 2015
Clinically relevant copy number variations detected in cerebral palsy.
Oskoui M et al. Nat Commun 2015 7949
Oskoui M et al. Nat Commun 2015 7949
De novo point mutations in patients diagnosed with ataxic cerebral palsy.
Parolin SR et al. Brain 2015 Jul (Pt 7) 1817-32
Parolin SR et al. Brain 2015 Jul (Pt 7) 1817-32
Copy number variations in cryptogenic cerebral palsy.
Segel R et al. Neurology 2015 Apr 21. (16) 1660-8
Segel R et al. Neurology 2015 Apr 21. (16) 1660-8
Genes determining the severity of cerebral palsy: the role of single nucleotide polymorphisms on the amount and structure of apolipoprotein E.
Lien E et al. Acta Paediatr. 2015 Jul (7) 701-6
Lien E et al. Acta Paediatr. 2015 Jul (7) 701-6
Cerebral palsy (CP) is a group of disorders that affect a person?s ability to move and maintain balance and posture. CP is the most common motor disability in childhood.
CDC estimates that an average of 1 in 323 children in the U.S. have CP
CDC estimates that an average of 1 in 323 children in the U.S. have CP
Check out genetic conditions and tests associated with cerebral palsy, from the NIH Genetic Testing Registry
from the NIH Genetic Testing Registry
Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy.
McMichael G et al. Mol. Psychiatry 2015 Feb (2) 176-82
McMichael G et al. Mol. Psychiatry 2015 Feb (2) 176-82
Systematic review: hereditary thrombophilia associated to pediatric strokes and cerebral palsy.
Torres VM et al. J Pediatr (Rio J) 2015 Jan-Feb (1) 22-9
Torres VM et al. J Pediatr (Rio J) 2015 Jan-Feb (1) 22-9
A diagnostic approach for cerebral palsy in the genomic era.
Lee RW et al. Neuromolecular Med. 2014 Dec (4) 821-44
Lee RW et al. Neuromolecular Med. 2014 Dec (4) 821-44
Clinical whole exome sequencing in child neurology practice.
Srivastava S et al. Ann. Neurol. 2014 Oct (4) 473-83
Srivastava S et al. Ann. Neurol. 2014 Oct (4) 473-83
Check out genes reported in relation to risk of cerebral palsy, from the HuGE Navigator
from the HuGE Navigator
Child apolipoprotein E gene variants and risk of cerebral palsy: Estimation from case-parent triads.
Stoknes M et al. Eur. J. Paediatr. Neurol. 2015 Jan 3.
Stoknes M et al. Eur. J. Paediatr. Neurol. 2015 Jan 3.
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