Acanthocytosis and spinocerebellar degeneration: A new association?

Movement Disorders

Volumn 12, Issue 3, 1997, Pages 456-459

  Tsai, C H ^a   Chen, R S ^a   Chang, H C ^a   Lu, C S ^a   Liao, K K ^a  

^a Chang Chang Memorial Hospital   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA TOCOPHEROL; BACLOFEN; CARBIDOPA PLUS LEVODOPA; CLONAZEPAM;

ACANTHOCYTOSIS; ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; DYSTONIA; HUMAN; MALE; PRIORITY JOURNAL; SPINOCEREBELLAR DEGENERATION;

EID: 0030914992     PISSN: 08853185     EISSN: None     Source Type: Journal    
DOI: 10.1002/mds.870120333     Document Type: Article

References (14)

1. 1 Bassen Fa, Kornzweig AI. Malformation of the erythrocytes in a case of atypical retinitis pigmentosa. Blood 1950 ; 5: 381–387.
2. 2 Mars H, Lewis LA, Robertson AL, et al. Familial hypolipoproteinemia: a genetic disorder of lipid metabolism with nervous system involvement. Am J Med 1969 ; 46: 886–900.
3. 3 Critchley EMR, Clark DB, Wikler A. Acanthocytosis and neurological disorder without abetalipoproteinemia. Arch Neurol 1968 ; 18: 134–140.
4. 4 Levine IM, Estes JW, Looney JM. Hereditary neurological disease with acanthocytosis. Arch Neurol 1968 ; 19: 403–409.
5. 5 Swash M, Schwartz MS, Cater ND, Heath R, Leak M, Togers KL. Benign X‐linked myopathy with acanthocytes (McLeod syndrome): its relationship to X‐linked muscular dystrophy. Brain 1983 ; 106: 717–733.
6. 6 Peppard RF, Lu CS, Chu NS, Teal P, Martin WRW, Calne DB. Parkinsonism with neuroacanthocytosis. Can J Neurol Sci 1990 ; 17: 298–301.
7. 7 Hardie RJ, Pullon HWH, Harding AE, et al. Neuroacanthocytosis. Brain 1991 ; 114: 13–49.
8. 8 Rinne JO, Daniel SE, Scaravilli F, Harding AE, Marsden CD. Nigral degeneration in neuroacanthocytosis. Neurology 1994 ; 44: 1629–1632.
9. 9 Rinne JO, Daniel SE, Scaravilli F, Pires M, Harding AD, Marsden CD. The neuropathological features of neuroacanthocytosis. Mov Disord 1994 ; 9: 297–304.
10. 10 Sahai T, Mawatari S, Iwashita H, Goto I, Kuroiwa Y. Choreoacanthocytosis: clues to clinical diagnosis. Arch Neurol 1981 ; 38: 335–338.
11. 11 Brooks DJ, Ibanez V, Playford ED, et al. Presynaptic and postsynaptic striatal dopaminergic function in neuroacanthocytosis: a positron emission tomographic study. Ann Neurol 1991 ; 30: 166–171.
12. 12 Sakai T, Antoku Y, Iwashita H, Goto I, Nagamatsu K, Shii H. Chorea‐acanthocytosis: abnormal composition of covalently bound fatty acids of erythrocyte membrane proteins. Ann Neurol 1991 ; 29: 664–669.
13. 13 Clark MR, Aminoff MJ, Chiu DT, Kuypers FA, Friend DS. Red cell deformability and lipid composition in two forms of acanthocytosis: enrichment of acanthocytic populations by density gradient centrifugation. J Lab Clin Med 1989 ; 113: 469–481.
14. 14 Kish SJ, Robitaille Y, Ball M, et al. Glycerophosphoethanolamine concentration is elevated in brain of patients with dominantly inherited olivopontocerebellar atrophy. Neurosci Lett 1990 ; 120: 209–211.