Cohort-based whole exome and whole genome sequencing and copy number variant
(CNV) studies have identified genetic etiologies for a sizable proportion of patients with …

Cerebral palsy (CP) is a clinical term used to describe a spectrum of movement and posture
disorders resulting from non-progressive disturbances in the developing fetal brain. The …

Movement Disorders in Childhood, Second Edition, provides the most up-to-date information
on the diseases and disorders that affect motor control, an important area of specialization …

Aim To provide a description of cerebral palsy (CP) registers globally, identify which aim to
report on CP epidemiology, and report similarities and differences across topics of …

Cerebral palsy (CP) is a broad diagnosis unbound by aetiology and is based on a clinical
examination demonstrating abnormalities of movement or posture. CP represents a static …

Background and Objectives To report on prevalence, associated impairments, severity, and
neuroimaging findings in children with ataxic cerebral palsy (CP). Methods In children coded …

Objective To report the prevalence of cerebral palsy (CP) in children with severe congenital
heart defects (sCHD) and the outcome/severity of the CP. Methods Population-based, data …

Aim To determine whether infants with intrauterine drug exposure (IUDE) are similarly at risk
for cerebral palsy (CP) as other high‐risk populations, whether CP classification differs …

Aim To describe the major congenital anomalies present in children with postneonatally
acquired cerebral palsy (CP), and to compare clinical outcomes and cause of postneonatally …

Background Infants with complex congenital heart disease are at increased risk of impaired
fetal brain growth, brain injury, and developmental impairments. The General Movement …