Young-onset Parkinson's disease: A clinical pathologic description of two siblings

Movement Disorders

Volumn 15, Issue 4, 2000, Pages 744-746

  Tabamo, Rowena Emilia J ^b   Fernandez, Hubert H ^a,b   Friedman, Joseph H ^b   Simon, David K ^c  

^a MEMORIAL HOSPITAL OF RHODE ISLAND   (United States)

^b BROWN UNIVERSITY   (United States)

^c HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARBIDOPA; CLOZAPINE; FERROUS SULFATE; HALOPERIDOL; LEVODOPA; NUCLEOTIDE;

ADULT; BLOOD ANALYSIS; CANADA; CASE REPORT; CLINICAL EXAMINATION; CLINICAL FEATURE; DOSE RESPONSE; DYSTONIA; EXON; FAMILY HISTORY; FEMALE; GENETIC ANALYSIS; HUMAN; IRON DEFICIENCY ANEMIA; MISSENSE MUTATION; MUSCLE RIGIDITY; NEUROLOGIC EXAMINATION; NOTE; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PALLIDOTOMY; PARKINSON DISEASE; PATHOLOGY; PORTUGAL; PRIORITY JOURNAL; PSYCHOSIS; SIBLING; TREMOR; VIDEORECORDING; VISUAL HALLUCINATION;

EID: 0033940605     PISSN: 08853185     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8257(200007)15:4<744::aid-mds1026>3.0.co;2-%23     Document Type: Note

References (30)

1. Schrag A, Ben-Shlomo Y, Brown R, Marsden CD. Young onset Parkinson's disease revisited, clinical features, natural history and mortality. Mov Disord 1998;13:885-894.
2. Ishikawa A, Tsuji S. Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism. Neurology 1996;47:160-166.
3. Quinn N, Critchley P, Marsden CD. Young onset Parkinson's disease. Mov Disord 1987;2:73-91.
4. Yokochi M. Nosological concept of juvenile parkinsonism with reference to the dopa-responsive syndrome. Adv Neurol 1993;60: 548-552.
5. Gibb WR, Lees AJ. A comparison of clinical and pathological features of young and old-onset Parkinson's disease. Neurology 1988;38:1402-1406.
6. Golbe LI. Young onset Parkinson's disease: a clinical review. Neurology 1991;41:168-173.
7. Rajput AH, Ryan MB. Parkinsonism and neurofibrillary tangle pathology in pigmented nuclei. Ann Neurol 1989;25:602-606.
8. Dwork AJ, Balmaceda C, Fazzini EA, MacCollin M, Cote L, Fahn S. Dominantly inherited, early-onset parkinsonism: neuropathology of a new form. Neurology 1993;43:69-74.
9. Takahashi H, Ohama E, Suzuki S, et al. Familial juvenile parkinsonism: clinical and pathologic study in a family. Neurology 1994; 44:437-441.
10. Ishikawa A, Takahashi H. Clinical and neuropathological aspects of autosomal recessive juvenile parkinsonism. J Neurol 1998;245 (suppl 3):4-9.
11. Glassor T. Genetics of Parkinson's disease. Ann Neurol 1998;44: 510-518.
12. Yamamura Y, Sobue I, Ando K, Iida M, Yanagi T, Kono C. Paralysis agitans of early onset with marked diurnal fluctuations of symptoms. Neurology 1973;23:239-244.
13. Mayer JM, Mikol J, Haguenau M, Dellanave J, Pepin B. Familial juvenile parkinsonism with multiple systems degenerations. A clinicopathological study. J Neurol Sci 1986;72:91-101.
14. Mori H, Kondo T, Yolochi M, et al. Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q. Neurology 1998;51:890-892.
15. Perry TL, Wright JM, Berry K, Hansen S, Perry TL Jr. Dominantly inherited apathy, central hypoventilation, and Parkinson's syndrome: clinical, biochemical, and neuropathologic studies of 2 new cases. Neurology 1990;40:1882-1887.
16. Gibb WRG, Lees AJ. A comparison of clinical and pathological features of young and old-onset Parkinson's disease. Neurology 1988;38:1402-1406.
17. Golbe LI, Di Iorio G, Bonavita V, Miller DC, Duvoisin RC. A large kindred with autosomal dominant Parkinson's disease. Ann Neurol 1990;27:276-282.
18. Meunter MD, Howard FM, Okazaki H, et al. A familial-parkinson-dementia syndrome. Neurology 1986;36:115.
19. Mizutani Y, Yokochi M, Oyanagi S. Juvenile parkinsonism: a case with first clinical manifestation at the age of six years and with neuropathological findings suggesting a new pathogenesis. Clin Neuropathol 1991;10:91-97.
20. Bhatia KP, Daniel SE, Marsden CD. Familial parkinsonism with depression: a clinicopathological study. Ann Neurol 1993;34:842-847.
21. Golbe LI, Lazzarini AM, Schwarz KO, Mark MH, Dickson DW, Duvoisin RC. Autosomal dominant parkinsonism with benign course and typical Lewy-body pathology. Neurology 1993;43:222-227.
22. Waters CH, Miller CA. Autosomal dominant Lewy-body parkinsonism in a four-generation family. Ann Neurol 1994;35:59-64.
23. Polymeropoulous MH, Lavendan C, Leroy E, et al. Alpha-synuclein gene identified in families with Parkinson's disease. Science 1997;276:2045-2047.
24. Kitada T, Asakawa S, Hattori N, et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 1998; 392:605-608.
25. Farrer M, Wavrant-De Vrieze F, Crook R, et al. Low-frequency of alpha-synuclein mutations in familial Parkinson's disease. Ann Neurol 1998;43:394-397.
26. Glasser T, Muller-Myhsok B, Wszolek Z, et al. A susceptibility locus for Parkinson's disease maps to chromosome 2 p13. Nat Genet 1998;18:265-266.
27. Leroy E, Bayer R, Aurburger G, et al. The ubiquitin pathway in Parkinson's disease. Nature 1998;395:451-452.
28. Kruger R, Kuhn W, Muller T, et al. Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease. Nat Genet 1998; 18:106-108.
29. Hattori N, Kitada T, Matsumine H, et al. Molecular genetic analysis of a novel parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the parkin gene in affected individuals. Ann Neurol 1998;44:935-941.
30. Simon DK, Pulst SM, Sutton JP, Browne SE, Beal MF, Johns D. Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutation. Neurology 1999;10: 1787-1793.