Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Copy number variations in cryptogenic cerebral palsy

29 Mar 2015

Abstract excerpt

OBJECTIVE: To determine the prevalence and characteristics of copy number variations (CNVs) in children with cerebral palsy (CP) of unknown etiology, comprising approximately 20% of the CP population. METHODS: Fifty-two participants (age 10.5 ± 7.8 years; Gross Motor Function Classification System scale 2.8 ± 1.3) with nonprogressive pyramidal and/or extrapyramidal signs since infancy and no identified etiology...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cerebral Palsy and Movement Disorders
Share to Genomic variations and chromosomal abnormalities
Share to Neurogenetic and Muscular Disorders Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 25817843
DOI: 10.1212/wnl.0000000000001494

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Copy number variations in cryptogenic cerebral palsyPMID 25817843Read ↗

Clinically relevant copy number variations detected in cerebral palsy.Semantic proximity Read ↗

De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy.Semantic proximity Read ↗

Insights From Genetic Studies of Cerebral PalsySemantic proximity Read ↗

Systematic Review on Genetic Variants in Children With Cerebral Palsy.Semantic proximity Read ↗

Cerebral palsy and related neuromotor disorders: Overview of genetic and genomic studies.Semantic proximity Read ↗

Hidden etiology of cerebral palsy: genetic and clinical heterogeneity and efficient diagnosis by next-generation sequencing.Semantic proximity Read ↗

Potential clinical applications of advanced genomic analysis in cerebral palsy.Semantic proximity Read ↗

Genetics of Cerebral Palsy: Diagnosis, Differential Diagnosis, and BeyondSemantic proximity Read ↗

Yield of clinically reportable genetic variants in unselected cerebral palsy by whole genome sequencingSemantic proximity Read ↗

The emerging genetic landscape of cerebral palsy.Semantic proximity Read ↗

Mendelian etiologies identified with whole exome sequencing in cerebral palsy.Semantic proximity Read ↗

Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsy.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.