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Article

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

Pediatric research - 1 Aug 2021

Rosello Monica, Caro-Llopis Alfonso, Orellana Carmen, Oltra Silvestre, Alemany-Albert Marta, Marco-Hernandez Ana V, Monfort Sandra, Pedrola Laia, Martinez Francisco, Tomás Miguel

Abstract excerpt

Cerebral palsy (CP) is a heterogeneous neurodevelopmental disorder that causes movement and postural disabilities. Recent research studies focused on genetic diagnosis in patients with CP of unknown etiology. The present study was carried out in 20 families with one family member affected with idiopathic CP. Chromosomal microarray and exome sequencing techniques were performed in all patients. Chromosomal...

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Cerebral Palsy
Child, Preschool
DNA Mutational Analysis
Genetic Heterogeneity
Genetic Markers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Genetic Testing

High-Throughput Nucleotide Sequencing

Predictive Value of Tests

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PMID: 33177673
DOI: 10.1038/s41390-020-01250-3

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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