Complicated hereditary spastic paraplegia with peripheral neuropathy, optic atrophy and mental retardation

Neuropediatrics

Volumn 31, Issue 4, 2000, Pages 214-217

  Miyama, S ^a   Arimoto, K ^a   Kimiya, S ^a   Tomi, H ^b  

^a Neurodevelopmental Intervention   (Japan)

^b Tomy Company Ltd   (Japan)

Author keywords

Epilepsy; Mental retardation; Optic atrophy; Peripheral neuropathy; Spastic paraplegia

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CORPUS CALLOSUM; DISEASE COURSE; EVOKED SOMATOSENSORY RESPONSE; FEMALE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MENTAL DEFICIENCY; MENTAL DEVELOPMENT; NUCLEAR MAGNETIC RESONANCE IMAGING; OPTIC NERVE ATROPHY; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL; SPASTICITY;

BRAIN; CHILD; CORPUS CALLOSUM; EVOKED POTENTIALS, SOMATOSENSORY; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MENTAL RETARDATION; OPTIC ATROPHY; PARAPLEGIA; PERIPHERAL NERVOUS SYSTEM DISEASES; SEVERITY OF ILLNESS INDEX;

EID: 0033780392     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2000-7462     Document Type: Article

References (13)

1. Hereditary spastic paraparesis (Strumpell-Lorrain)
2. Clinically silent dysfunction of dorsal columns and dorsal spinocerebellar tracts in hereditary spastic paraparesis
3. Hereditary spastic paraparesis with dementia, amyotrophy and peripheral neuropathy. A neuropathological study
4. Autosomal dominant familial spastic paraplegia: Tight linkage to chromosome 15 q
5. Somatosensory evoked potentials and the dorsal column myth
6. Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14 q
7. Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity
8. Three patients of complicated form of autosomal recessive hereditary spastic paraplegia associated with hypoplasia of the corpus callosum
9. Multiple system atrophies: A neuropathological and neurochemical study
10. Familial spastic paraplegia with mental impairment and thin corpus callosum
11. Motor and somatosensory evoked potentials in hereditary spastic paraplegia
12. Hereditary spastic paraplegia with a thin corpus callosum and thalamic involvement in Japan
13. Strumpell's familial spastic paraplegia: An electrophysiological demonstration of selective central distal axonopathy