Genetic and Genomic Insights Into Cerebral Palsy: Relevance for Precision Diagnosis and Personalised Outcomes

Abstract excerpt

Introduction: Cerebral palsy (CP) is a debilitating heterogeneous clinical condition manifesting with non-progressive neurodevelopmental difficulties of posture and movement. Multiple causes are associated with the onset of CP, all directly or indirectly linked with the structural and/or functional damage to the developing brain. The majority of the causes are acquired during or soon after childbirth, notably hypo...

Topics

Open a Topic to create a Post that cites this publication.

• Cerebral Palsy and Movement Disorders
• Genomics and Rare Diseases
• Neurogenetic and Muscular Disorders Research

Identifiers and source

Literature Corpus work

74193fa2-f983-58f5-8e8e-57b36abaa5fc

DOI

10.1177/09760016261475011