Infantile neuroaxonal dystrophy (Seitelberger's disease)

Developmental Medicine and Child Neurology

Volumn 44, Issue 12, 2002, Pages 849-851

  Gordon, Neil ^a  

^a Huntlywood   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

5 HYDROXYINDOLEACETIC ACID; ALPHA N ACETYLGALACTOSAMINIDASE; ANTICONVULSIVE AGENT; HOMOVANILLIC ACID; PANTOTHENATE KINASE; PROTEIN; PROTEOLIPID PROTEIN; SPASMOLYTIC AGENT;

ATAXIA; AUTOPSY; CEREBROSPINAL FLUID; CHILD DEATH; CHROMOSOME 20P; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; CORPUS CALLOSUM; DEMENTIA; DIFFERENTIAL DIAGNOSIS; ELECTROENCEPHALOGRAPHY; ELECTROMYOGRAPHY; ELECTRON MICROSCOPY; ELECTRORETINOGRAM; EYE MOVEMENT DISORDER; GENE; GENE MUTATION; HALLERVORDEN SPATZ DISEASE; HEARING IMPAIRMENT; HUMAN; INFANTILE HYPOTONIA; MENTAL DETERIORATION; METACHROMATIC LEUKODYSTROPHY; NERVE BIOPSY; NERVE DEGENERATION; NEUROAXONAL DYSTROPHY; NEUROPATHOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; NYSTAGMUS; ONSET AGE; OPTIC NERVE ATROPHY; PRIORITY JOURNAL; PROTEIN EXPRESSION; PYRAMIDAL NERVE CELL; RECESSIVE INHERITANCE; REVIEW; SEIZURE; SPASTICITY; STRABISMUS; SYMPTOM; VISUAL DISORDER; VISUAL IMPAIRMENT;

BRAIN; DIAGNOSIS, DIFFERENTIAL; ELECTROENCEPHALOGRAPHY; EVOKED POTENTIALS, AUDITORY, BRAIN STEM; EVOKED POTENTIALS, VISUAL; HALLERVORDEN-SPATZ SYNDROME; HUMANS; MAGNETIC RESONANCE IMAGING; NEUROAXONAL DYSTROPHIES; SEIZURES;

EID: 0036890420     PISSN: 00121622     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0012162201003036     Document Type: Review

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