Article
A phenotypic paradigm for cerebral palsy genetics.
American journal of human genetics - 3 Sept 2026
Arterbery Adam S, Gargano Michael A, Bagley Anita, Chandrabose Sundaramurthi Jagadish, Rekerle Lauren, Ordaz-Robles Thania, Danis Daniel, Graefe Adam S L, Arenas-Díaz Ana L, Bauer Jeremy P, Blau Hannah, Carmody Leigh, Carroll Kristen I, Davis Janice, Giampietro Philip F, Gustafson Anxhela Gjyshi, Hernandez Monserat, Jacobsen Julius O B, Lemhouse Paige, Millet David, Mukherjee Shubhra, Nairne Patrick S, Nice Emily, Plotkin Talia, Powell Kenneth, Ramlow Lukas, Raney Ellen M, Shingle Mallory, Smedley Damian, Smith Peter A, Soliman Demiana A, Westberry David E, Davids Jon R, Robinson Peter N
Abstract excerpt
Cerebral palsy (CP) represents a clinically and etiologically heterogeneous group of permanent but not unchanging disorders of movement, posture, and motor function resulting from non-progressive disturbances of the developing fetal or infant brain. Pathogenic variants in Mendelian disease-associated genes can be found in a subset of individuals with CP, with variants deemed causal of CP having been published for...
Read the complete abstract on PubMedTopics
- Humans
- Cerebral Palsy
- Phenotype