Hereditary spastic paraparesis and psychosis

European Journal of Neurology

Volumn 13, Issue 8, 2006, Pages 874-879

  McMonagle, P ^a,c   Hutchinson, M ^a   Lawlor, B ^b  

^a ST VINCENT S UNIVERSITY HOSPITAL   (Ireland)

^b TRINITY COLLEGE DUBLIN   (Ireland)

^c SOUTHAMPTON GENERAL HOSPITAL   (United Kingdom)

Author keywords

Hereditary spastic paraparesis; Kjellin's syndrome; Operational Diagnostic Criteria Checklist; Schizophrenia; SPG4

Indexed keywords

ADULT; AGED; ARTICLE; FAMILY; FEMALE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; IRELAND; KJELLIN SYNDROME; MAJOR CLINICAL STUDY; MALE; MANIA; POPULATION; PRIORITY JOURNAL; PSYCHOSIS; SCHIZOAFFECTIVE PSYCHOSIS; SCHIZOPHRENIA; SYNDROME;

ADENOSINE TRIPHOSPHATASES; ADULT; AGED; FAMILY HEALTH; FEMALE; HEAT-SHOCK PROTEINS; HUMANS; IRELAND; MALE; NEUROPSYCHOLOGICAL TESTS; PSYCHOTIC DISORDERS; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 33746451665     PISSN: 13515101     EISSN: 14681331     Source Type: Journal    
DOI: 10.1111/j.1468-1331.2006.01379.x     Document Type: Article

References (34)

1. Harding AE. Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families. Journal of Neurology Neurosurgery & Psychiatry 1981; 44: 871-883.
2. Baraitser M. Pyramidal tract disorders. In: Baraitser M., ed. The Genetics of Neurological Disorders, 3rd edn. Oxford: Oxford University Press, 1997: 200-209.
3. Harding AE. Classification of the hereditary ataxias and paraplegias. Lancet 1983; 1: 1151-1155.
4. Reid E. Pure hereditary spastic paraplegia. Journal of Medical Genetics 1997; 34: 499-503.
5. Pridmore S, Rao G, Abusah P. Hereditary spastic paraplegia with dementia. Australian & New Zealand Journal of Psychiatry 1995; 29: 678-682.
6. Webb S, Coleman D, Byrne P et al. Autosomal dominant hereditary spastic paraparesis with cognitive loss linked to chromosome 2p. Brain 1998; 121: 601-609.
7. Heinzlef O, Paternotte C, Mahieux F et al. Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p. Journal of Medical Genetics 1998; 35: 89-93.
8. Byrne P, McMonagle P, Webb S et al. Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p. Neurology 2000; 54: 1510-1517.
9. White KD, Ince PG, Lusher M et al. Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation. Neurology 2000; 55: 89-94.
10. Tallaksen CM, Guichart-Gomez E, Verpillat P et al. Subtle cognitive impairment but no dementia in patients with spastin mutations. Archives of Neurology 2003; 60: 1113-1118.
11. McMonagle P, Byrne P, Hutchinson M. Further evidence of dementia in SPG4-linked autosomal dominant hereditary spastic paraplegia. Neurology 2004; 62: 407-410.
12. McMonagle P, Webb S, Hutchinson M. The prevalence of "pure" autosomal dominant hereditary spastic paraparesis in the island of Ireland. Journal of Neurology Neurosurgery & Psychiatry 2002; 72: 43-46.
13. McGuffin P, Farmer A, Harvey I. A polydiagnostic application of operational criteria in studies of psychotic illness. Archives of General Psychiatry 1991; 48: 764-770.
14. Williams J, Farmer AE, Ackenheil M et al. A multi-centre inter-rater reliability study using the OPCRIT computerised diagnostic system. Psychological Medicine 1996; 26: 775-783.
15. Spitzer R, Endicott J, Robins E. Research diagnostic criteria; rationale and reliability. Archives of General Psychiatry 1978; 35: 773-782.
16. Roth M, Tym E, Mountjoy CQ et al. CAMDEX: a standardised instrument for the diagnosis of mental disorder in the elderly with special reference to the early detection of dementia. British Journal of Psychiatry 1986; 149: 698-709.
17. 6Folstein MF, Folstein SE, McHugh PR. "Mini-Mental State": a practical method for grading the cognitive state of patients for the clinician. Journal of Psychiatric Research 1975; 12: 189-198.
18. Webb S, Patterson V, Hutchinson M. Two families with autosomal recessive spastic paraplegia, pigmented maculopathy, and dementia. Journal of Neurology Neurosurgery & Psychiatry 1997; 63: 628-632.
19. McMonagle P, Byrne PC, Fitzgerald B et al. Phenotype of AD-HSP due to mutations in the SPAST gene: comparison with AD-HSP without mutations. Neurology 2000; 55: 1794-1800.
20. Hughes C, Byrne P, Webb S et al. A new locus for autosomal recessive 'complicated' hereditary spastic paraparesis on chromosome 14q. Neurology 2001; 56: 1230-1233.
21. Gelder M, Gath D, Mayou R, Cowen P. Schizophrenia and schizophrenia-like disorders. In: Gelder M, Gath D, Mayou R, Cowen P., eds. Oxford Textbook of Psychiatry, 3rd edn. Oxford: Oxford University Press, 1996: 267.
22. Hwang TJ, Masterman DM, Ortiz F et al. Mild cognitive impairment is associated with characteristic neuropsychiatric symptoms. Alzheimer's Disease and Associated Disorders 2004; 18: 17-22.
23. Rao V, Lyketsos CG. Delusions in Alzheimer's disease: a review. Journal of Neuropsychiatry and Clinical Neurosciences 1998; 10: 373-382.
24. Turner TH. Schizophrenia and mental handicap: an historical review, with implications for further research. Psychological Medicine 1989; 19: 301-314.
25. Nielsen JE, Johnsen B, Koefoed P et al. Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation. European Journal of Neurology 2004; 11: 817-824.
26. Sperfeld AD, Kassubek J, Crosby AH et al. Complicated hereditary spastic paraplegia with thin corpus callosum: variation of phenotypic expression over time. Journal of Neurology 2004; 251: 1285-1287.
27. Wilkinson PA, Simpson MA, Bastaki L et al. A new locus for autosomal recessive hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1-12q14. Journal of Medical Genetics 2005; 42: 80-82.
28. Yanase D, Komai K, Hamaguchi T et al. Hereditary spastic paraplegia with frontal lobe dysfunction. A clinicopathologic study. Neurology 2004; 63: 2149-2152.
29. Lindsey JC, Lusher ME, McDermott CJ et al. Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis. Journal of Medical Genetics 2000; 37: 759-765.
30. Bundey S. Extrapyramidal disorders and dyskinesias. In: Bundey S., ed. Genetics and Neurology, 2nd edn. Edinburgh: Churchill Livingstone, 1992: 132.
31. Doheny DO, Brin MF, Morrison CE et al. Phenotypic features of myoclonus dystonia in three kindreds. Neurology 2002; 59: 1187-1196.
32. Adachi N, Arima K, Asada T et al. Dentatorubral-pallidoluysian atrophy (DRPLA) presenting with psychosis. The Journal of Neuropsychiatry and Clinical Neurosciences 2001; 13: 258-260.
33. Turner R, Schiavetto A. The cerebellum in schizophrenia: a case of intermittent ataxia and psychosis - clinical, cognitive and neuroanatomical correlates. The Journal of Neuropsychiatry and Clinical Neurosciences 2004; 16: 400-408.
34. Jabelensky A. The 100-year epidemiology of schizophrenia. Schizophrenia Research 1997; 28: 111-125.