[{"n": "Acute flaccid myelitis", "u": "/e/neurological-disorders-in-children/acute-flaccid-myelitis/", "s": "A rare spinal cord condition mainly affecting children."}, {"n": "Amblyaudia", "u": "/e/neurological-disorders-in-children/amblyaudia/", "s": "A brain-based hearing disorder with asymmetric ear performance."}, {"n": "Childhood disintegrative disorder", "u": "/e/neurological-disorders-in-children/childhood-disintegrative-disorder/", "s": "Rare childhood disorder with late regression of acquired skills."}, {"n": "DHX30 syndrome", "u": "/e/neurological-disorders-in-children/dhx30-syndrome/", "s": "A rare neurodevelopmental disorder caused by DHX30 gene mutations."}, {"n": "Idiopathic childhood occipital epilepsy of Gastaut", "u": "/e/neurological-disorders-in-children/idiopathic-childhood-occipital-epilepsy-of-gastaut/", "s": "A rare childhood epilepsy with brief, frequent visual seizures."}, {"n": "Jordan's syndrome", "u": "/e/neurological-disorders-in-children/jordan-s-syndrome/", "s": "A rare neurodevelopmental disorder from PPP2R5D mutations."}, {"n": "Krabbe disease", "u": "/e/neurological-disorders-in-children/krabbe-disease/", "s": "A rare, fatal leukodystrophy from GALC enzyme deficiency."}, {"n": "Lysosomal storage disease", "u": "/e/neurological-disorders-in-children/lysosomal-storage-disease/", "s": "Rare inherited disorders from lysosomal enzyme defects."}, {"n": "Metachromatic leukodystrophy", "u": "/e/neurological-disorders-in-children/metachromatic-leukodystrophy/", "s": "A genetic disorder causing progressive demyelination and neurological decline."}, {"n": "Modified Checklist for Autism in Toddlers", "u": "/e/neurological-disorders-in-children/modified-checklist-for-autism-in-toddlers/", "s": "Screens toddlers for autism spectrum disorder risk."}, {"n": "Myoclonic astatic epilepsy", "u": "/e/neurological-disorders-in-children/myoclonic-astatic-epilepsy/", "s": "A generalized idiopathic epilepsy with myoclonic and atonic seizures."}, {"n": "Neonatal encephalopathy", "u": "/e/neurological-disorders-in-children/neonatal-encephalopathy/", "s": "A brain injury syndrome from birth asphyxia in term newborns."}, {"n": "Panayiotopoulos syndrome", "u": "/e/neurological-disorders-in-children/panayiotopoulos-syndrome/", "s": "A benign age-related focal seizure disorder of childhood with autonomic symptoms."}, {"n": "Pervasive developmental disorder", "u": "/e/neurological-disorders-in-children/pervasive-developmental-disorder/", "s": "A former category of developmental disorders affecting socialization and communication."}, {"n": "Pervasive developmental disorder not otherwise specified", "u": "/e/neurological-disorders-in-children/pervasive-developmental-disorder-not-otherwise-specified/", "s": "Historic diagnosis now subsumed under autism spectrum disorder."}, {"n": "Recurrent painful ophthalmoplegic neuropathy", "u": "/e/neurological-disorders-in-children/recurrent-painful-ophthalmoplegic-neuropathy/", "s": "Rare disorder with recurrent headaches and ocular nerve palsy."}, {"n": "Rett syndrome", "u": "/e/neurological-disorders-in-children/rett-syndrome/", "s": "A genetic neurodevelopmental disorder affecting mostly girls."}, {"n": "Spectrum 10K", "u": "/e/neurological-disorders-in-children/spectrum-10k/", "s": "Cancelled UK study of genetic and environmental factors in autism."}, {"n": "Spinocerebellar ataxia type 1", "u": "/e/neurological-disorders-in-children/spinocerebellar-ataxia-type-1/", "s": "A rare inherited disorder causing progressive cerebellar ataxia and neurodegeneration."}, {"n": "Spinocerebellar ataxia type 13", "u": "/e/neurological-disorders-in-children/spinocerebellar-ataxia-type-13/", "s": "A rare, progressive cerebellar ataxia with epilepsy and mental retardation."}, {"n": "Stereotypic movement disorder", "u": "/e/neurological-disorders-in-children/stereotypic-movement-disorder/", "s": "A childhood motor disorder of repetitive, impairing movements."}, {"n": "Tay–Sachs disease", "u": "/e/neurological-disorders-in-children/tay-sachs-disease/", "s": "Fatal inherited disorder destroying nerve cells, common in certain populations."}, {"n": "Transient hyperammonemia of the newborn", "u": "/e/neurological-disorders-in-children/transient-hyperammonemia-of-the-newborn/", "s": "Idiopathic hyperammonemia in preterm newborns, treatable with dialysis."}]