Generalized freezing in Hallervorden-Spatz syndrome: Case report

European Journal of Neurology

Volumn 6, Issue 4, 1999, Pages 509-513

  Guimarães, João ^a   Santos, J Vale ^a  

^a HOSPITAL EGAS MONIZ   (Portugal)

Author keywords

Eye of the tiger sign; Freezing; Hallervorden Spatz syndrome

Indexed keywords

ADULT; ARTICLE; BODY EQUILIBRIUM; CASE REPORT; CLINICAL FEATURE; FEMALE; GLOBUS PALLIDUS; HALLERVORDEN SPATZ DISEASE; HUMAN; MOTOR DYSFUNCTION; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; VOLUNTARY MOVEMENT;

EID: 0032779722     PISSN: 13515101     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1468-1331.1999.640509.x     Document Type: Article

References (41)

1. Achiron A, Ziv I, Goren M, Goldberg H, Zoldan Y, Sroka H, Mclamed E (1993). Primary progressive freezing gait. Movement Disord 8:293-297.
2. Ambrosetto P, Nonni R, Bacci A, Gobbi G (1992). Late onset familial Hallervorden-Spatz disease: MR findings in two sisters. AJNR 13:394-396.
3. Angelini L, Nardocci N, Rumi V, Zorzi C, Strada L, Savoiardo M (1992). Hallervorden-Spatz disease: clinical and MRI study of II cases diagnosed in life. J Neurol 239:417-425.
4. Atchison PR, Thompson PD, Frackowiak RSJ, Marsden CD (1993). The syndrome of gait ignition failure: a report of six cases. Movement Disord 8:285-292.
5. Ballard PA, Tetrud JW, Langston JW (1985). Permanent human Parkinsonism due to 1-methyl-4-phenyl-1,2,3,6, tetrahydropyridine (MPTP): seven cases. Neurology 35:949-956.
6. Benecke R, Rothwell JC, Dick JPR, Day BL, Marsdcn CD (1987), Disturbance of sequential movements in patients with Parkinson's disease. Brain 110:361-379.
7. Boghen D (1997). Apraxia of lid opening. Neurology 48:1491-1503.
8. Brotchie P, Iansek R, Horne MK (1991). Motor function of the monkey globus pallidus. Brain 114:1685-1702.
9. Brown JW (1972). Aphasia, apraxia and agnosia: clinical and theoretical aspects. Springfield, Illinois, Charles C. Thomas.
10. Collins SJ, Ahlskog JE, Parisi JE, Maraganore DM (1995). Progressive supranuclear palsy: neuropathologically based diagnostic clinical criteria. J Neurol Neurosurg Psychiat 58:167-173.
11. Curran T, Lang AE (1994). Parkinsonian syndromes associated with hydrocephalus: case reports. A review of the literature and pathophysiologic hypotheses. Movement Disord 9:508-520.
12. Davie CA, Barker GJ, Machado C, Miller DM, Lees AJ (1997). Proton magnetic resonance spectroscopy in Steele-Richardson-Olszewski syndrome. Movement Disord 5:767-771.
13. Dooling EC, Schoewe WC, Richardson EP (1974). Hallervorden-Spatz syndrome. Arch Neurol 30:70-83.
14. Drayer B, Burger P, Darwin R, Riderer S, Herfkens R, Johnson GA (1986). MRI of brain iron. AJR 147:103-110.
15. Eidelberg D, Sotrel A, Joachim C, Selkoe D, Forman A, Pendlebury WW, Perl, DP (1987). Adult onset Hallervorden-Spatz disease with neurofibrillary pathology. Brain 110:993-1013.
16. Fahn S (1995). The freezing phenomenon in Parkinsonism. Adv Neurol 67:53-63.
17. Fève AP, Fenelon G, Wallays C, Rémy P, Guillard A (1993). Axial motor disturbances after hypoxic lesions of the globus pallidus. Movement Disord 8:321-326.
18. Giladi N, McMahon D. Przedborski S, Flaster E, Guillory S, Kostic V, Fahn S (1992). Motor blocks in Parkinson's disease. Neurology 42:333-339.
19. Giladi N, Kao K, Fahn S (1997). Freezing phenomenon in patients with Parkinsonian syndromes. Movement Disord 12:302-305.
20. Halsband U, Ito N, Tanji J, Freund H-J (1993). The role of pre-motor cortex and the supplementary motor area in the temporal control of movement in man. Brain 116:243-266.
21. Hoover JE, Strick PL (1993). Multiple output channels in the basal ganglia. Science 259:819-821.
22. Imai H, Nakamura T, Kondo T, Narabayashi H (1993). Dopa-unresponsive pure akinesia or freezing. A condition within a wide spectrum of PSP? Adv Neurol 60:622-625.
23. Jankovic J, Kirkpatrick JB, Blomquist KA, Langlais PJ, Bird ED (1985). Late-onset Hallervorden-Spatz disease presenting as familial parkinsonism. Neurology 35:227-234.
24. Lees AJ (1987). The Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy). In: Movement Disorders 2 (editors) Marsden CD, Fahn S. London, Butterworth. pp. 272-287.
25. Litvan I, Agid Y, Calne D, et al. (1996). Clinical research criteria tor the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP International Workshop. Neurology 47:1-9.
26. nd edition). New York, Basic Books, Inc., Publishers, pp. 215-226.
27. Martin JP (1967). The Basal Ganglia and Posture. Philadelphia, Lippincott.
28. Matsuo H, Takashima H, Kishikawa M, Kinoshita I, Mori M, Tsujihata M, Nagataki S (1991). Pure akinesia: an atypical manifestation of progressive supranuclear palsy. J Neurol Neurosurg Psychiat 54:397-400.
29. Mestre D, Blin O, Serratrice G (1992). Contrast sensitivity increased in a case of non-Parkinsonian freezing gait. Neurology 42:189-194.
30. Mizusawa H, Mochizuki A, Ohkoshi N, Yoshizawa K, Kanazawa I, Imai H (1993). Progressive supranuclear palsy presenting with pure akinesia. Adv Neurol 60:618-621.
31. Mutoh K, Okuno T, Ito M, Nakano S, Mikawa H, Fujisawa I, Asato R (1988). MR imaging of a group I case of Hallervorden-Spatz disease. J Comput Assist Tomography 12(5):851-852.
32. Narabayashi H, Imai H, Yokochi M, Hirayama K, Nakamura R (1976). Cases of pure akinesia without rigidity and tremor and with no effect by L-dopa therapy. In: Advances in Parkinsonism (editors) Birkmayer W, Hornykiewicz O. Basel, Roche. pp. 335-342.
33. Nutt JG, Marsden CD, Thompson PD (1993). Human walking und higher-level gait disorders, particularly in the elderly. Neurology 43:268-279.
34. Orrel RW, Amrolia PJ, Heald A, Cleland PG, Owen JS, Morgan-Hughes JA, et al. (1995). Acanthocytosis, retinitis pigmentosa and pallidal degeneration: a report of three patients, including the second reported case with hypoprebetalipoproteinemia (HARP syndrome). Neurology 45:487-492.
35. Østergaard JR, Christensen T, Hansen KN (1994). In vivo diagnosis of Hallervorden-Spatz disease. Devel Med Child Neurol 37:827-833.
36. Rafal R, Inhoff AW, Friedman J, Bernstein E (1987). Programming and execution of sequential movements in Parkinson's disease. J Neurol Neurosurg Psychiat 50:1267-1273.
37. Savoiardo M, Halliday WC, Nardocci N, et al. (1993). Hallervorden-Spatz disease: MR and pathologic findings. AJNR 14:155-162.
38. Schaffert DA, Johnson SD, Jonhson PC, Drayer BP (1989). Magnetic resonance in pathologically proven Hallervorden-Spatz disease. Neurology 39:440-442.
39. Sethi KD, Adams RJ, Loring DW, El Gammal T (1988). Hallervorden-Spatz syndrome: clinical and magnetic resonance imaging correlations. Ann Neurol 24:692-694.
40. Swaiman KF (1991). Hallervorden-Spatz syndrome and brain iron metabolism, Arch Neurol 48:1285-1293.
41. Taylor TD, Litt M, Kramer P, Pandolfo M, Angelini L, Nardocci N, et al. (1996). Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13. Nat Genet 14:479-481.