History |
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No risk factors for CP such as: prematurity, low birthweight, multiple births, hypoglycemia, jaundice and kernicterus, intrapartum asphyxia, intracranial hemorrhage, infection, stroke, or head injuries |
Positive family history of CP |
Fluctuation in motor symptoms |
Paroxysmal symptoms in relation to time of day, diet/fasting, or activity |
Progressive neurological symptoms |
Regression of milestones |
Examination |
Dysmorphic features |
Isolated motor dysfunction such as isolated ataxia or isolated hypotonia without dystonia or spasticity |
Peripheral nervous system abnormalities: absent reflexes, sensory signs |
Eye movement abnormalities (e.g., oculogyria, oculomotor apraxia, or paroxysmal saccadic eye-head movements) |
Optic atrophy/retinopathy |
CP- cerebral palsy