Cerebral Palsy
Cerebral palsy: Public Health and Genomic Insights - March 25, 2015
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 RegistryWhole-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 NavigatorChild 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.
.png)
No hay comentarios:
Publicar un comentario