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Volumn 6, Issue 5, 2002, Pages 243-247

Pantothenate kinase-associated neurodegeneration (Hallervorden-Spatz syndrome)

Author keywords

Causes; Nomenclature; PKAN; Symptoms; Treatment

Indexed keywords

ANTICONVULSIVE AGENT; ANTIOXIDANT; BACLOFEN; BOTULINUM TOXIN; CHOLINERGIC RECEPTOR BLOCKING AGENT; COENZYME A; CYSTEINE; IRON; LEVODOPA; PANTOTHENATE KINASE; PANTOTHENIC ACID;

EID: 0037000025     PISSN: 10903798     EISSN: None     Source Type: Journal    
DOI: 10.1053/ejpn.2002.0606     Document Type: Review
Times cited : (56)

References (48)
  • 1
    • 0029803683 scopus 로고    scopus 로고
    • Naming of syndromes and unethical activities: The case of Hallervorden and Spatz
    • Harper P. Naming of syndromes and unethical activities: the case of Hallervorden and Spatz. Lancet 1996; 348: 1224-1225.
    • (1996) Lancet , vol.348 , pp. 1224-1225
    • Harper, P.1
  • 2
    • 0034839088 scopus 로고    scopus 로고
    • Julius Hallervorden's wartime activities: Implication for science under dictatorship
    • Shevell MI, Peiffer J. Julius Hallervorden's wartime activities: implication for science under dictatorship. Pediatr Neurol 2001; 25: 162-165.
    • (2001) Pediatr. Neurol. , vol.25 , pp. 162-165
    • Shevell, M.I.1    Peiffer, J.2
  • 3
    • 0030583754 scopus 로고    scopus 로고
    • Naming of syndromes
    • Morrison P. Naming of syndromes. Lancet 1996; 348: 1662.
    • (1996) Lancet , vol.348 , pp. 1662
    • Morrison, P.1
  • 4
    • 0030583754 scopus 로고    scopus 로고
    • Naming of syndromes
    • Shevell M. Naming of syndromes. Lancet 1996; 348: 1662.
    • (1996) Lancet , vol.348 , pp. 1662
    • Shevell, M.1
  • 5
    • 0030583756 scopus 로고    scopus 로고
    • Naming of syndromes
    • Jacby R, Oppenheimer C. Naming of syndromes. Lancet 1996; 348: 1662.
    • (1996) Lancet , vol.348 , pp. 1662
    • Jacby, R.1    Oppenheimer, C.2
  • 6
    • 0034996072 scopus 로고    scopus 로고
    • Four siblings with Hallervorden-Spatz disease
    • Vaher U, Napa A, Nurmiste A et al. Four siblings with Hallervorden-Spatz disease. Brain Dev 2001; 23: 236-239.
    • (2001) Brain Dev. , vol.23 , pp. 236-239
    • Vaher, U.1    Napa, A.2    Nurmiste, A.3
  • 7
    • 0034935036 scopus 로고    scopus 로고
    • A novel pantothenate kinase gene is defective in Hallervorden-Spatz syndrome
    • Zhou B, Westaway SK, Levinson B et al. A novel pantothenate kinase gene is defective in Hallervorden-Spatz syndrome. Nature Genet 2001; 28: 345-349.
    • (2001) Nature Genet. , vol.28 , pp. 345-349
    • Zhou, B.1    Westaway, S.K.2    Levinson, B.3
  • 8
    • 0029434793 scopus 로고
    • The nosology of Hallervorden-Spatz disease
    • Halliday W. The nosology of Hallervorden-Spatz disease. J Neurol Sci 1995; 134: 84-91.
    • (1995) J. Neurol. Sci. , vol.134 , pp. 84-91
    • Halliday, W.1
  • 9
    • 0343776132 scopus 로고    scopus 로고
    • Hallervorden-Spatz disease: Two new early childhood onset cases
    • Peña JA, Molina O, Cardozo J. Hallervorden-Spatz disease: two new early childhood onset cases. J Child Neurol 2000; 15: 30-32.
    • (2000) J. Child Neurol. , vol.15 , pp. 30-32
    • Peña, J.A.1    Molina, O.2    Cardozo, J.3
  • 11
    • 0033897338 scopus 로고    scopus 로고
    • Late adult onset chorea with typical pathology of Hallervorden-Spatz syndrome
    • Grimes DA, Lang AE, Bergeron C. Late adult onset chorea with typical pathology of Hallervorden-Spatz syndrome. J Neurol Neurosurg Psychiatry 2000; 69: 392-395.
    • (2000) J. Neurol. Neurosurg. Psychiatry , vol.69 , pp. 392-395
    • Grimes, D.A.1    Lang, A.E.2    Bergeron, C.3
  • 12
    • 0028333849 scopus 로고
    • Complex tics, stereotypes, and compulsive behaviour as clinical presentation of a juvenile progressive dystonia suggestive of Hallervorden-Spatz disease
    • Nardocci N, Rumi, V Angelini L et al. Complex tics, stereotypes, and compulsive behaviour as clinical presentation of a juvenile progressive dystonia suggestive of Hallervorden-Spatz disease. Mov Disord 1994; 9: 369-371.
    • (1994) Mov. Disord. , vol.9 , pp. 369-371
    • Nardocci, N.1    Rumi, V.2    Angelini, L.3
  • 13
    • 0028153393 scopus 로고
    • Optic atrophy as the presenting sign in Hallervorden-Spatz syndrome
    • Casteels I, Spileers W, Swinnen T et al. Optic atrophy as the presenting sign in Hallervorden-Spatz syndrome. Neuropediatrics 1994; 25: 265-267.
    • (1994) Neuropediatrics , vol.25 , pp. 265-267
    • Casteels, I.1    Spileers, W.2    Swinnen, T.3
  • 15
    • 0033544428 scopus 로고    scopus 로고
    • Hallervorden Spatz disease and acanthocytes
    • Muthane UB, Shetty R, Panda K et al. Hallervorden Spatz disease and acanthocytes. Neurology 1999; 53: 32A.
    • (1999) Neurology , vol.53
    • Muthane, U.B.1    Shetty, R.2    Panda, K.3
  • 16
    • 0029154352 scopus 로고
    • Myopathic involvement in two cases of Hallervorden-Spatz disease
    • Malandrini A, Bonuccelli U, Parrotta E et al. Myopathic involvement in two cases of Hallervorden-Spatz disease. Brain Dev 1995; 17: 286-290.
    • (1995) Brain Dev. , vol.17 , pp. 286-290
    • Malandrini, A.1    Bonuccelli, U.2    Parrotta, E.3
  • 17
    • 0035174081 scopus 로고    scopus 로고
    • What's new in neurogenetics? Focus on neurodegenerative disorders
    • Suri M. What's new in neurogenetics? Focus on neurodegenerative disorders. Eur J Paediatr Neurol 2001; 5: 221-224.
    • (2001) Eur. J. Paediatr. Neurol. , vol.5 , pp. 221-224
    • Suri, M.1
  • 20
    • 0033709213 scopus 로고    scopus 로고
    • The eye-of-the-tiger sign
    • Guillerman RP. The eye-of-the-tiger sign. Radiology 2000; 217: 895-896.
    • (2000) Radiology , vol.217 , pp. 895-896
    • Guillerman, R.P.1
  • 21
    • 0033897317 scopus 로고    scopus 로고
    • Constellation of findings on nigrostriatal system in case of Hallervorden-Spatz disease
    • Hermann W, Barthel H, Reuter M, et al. Constellation of findings on nigrostriatal system in case of Hallervorden-Spatz disease. Nervenarzt 2000; 71: 660-665.
    • (2000) Nervenarzt , vol.71 , pp. 660-665
    • Hermann, W.1    Barthel, H.2    Reuter, M.3
  • 22
    • 0032586053 scopus 로고    scopus 로고
    • Iron deposits in the subthalamic nuclei in Hallervorden-Spatz disease
    • Müller T, Amoiridis G, Kuhn W, Przuntek H. Iron deposits in the subthalamic nuclei in Hallervorden-Spatz disease. Eur Neurol 1999; 42: 240-241.
    • (1999) Eur. Neurol. , vol.42 , pp. 240-241
    • Müller, T.1    Amoiridis, G.2    Kuhn, W.3    Przuntek, H.4
  • 23
    • 0034850470 scopus 로고    scopus 로고
    • Cranial MRI changes may precede symptoms in Hallervorden-Spatz syndrome
    • Hayflick S, Penzien JM, Michl W et al. Cranial MRI changes may precede symptoms in Hallervorden-Spatz syndrome. Pediatr Neurol 2001; 25: 166-169.
    • (2001) Pediatr. Neurol. , vol.25 , pp. 166-169
    • Hayflick, S.1    Penzien, J.M.2    Michl, W.3
  • 24
    • 0034845760 scopus 로고    scopus 로고
    • Iron in the Hallervorden-Spatz syndrome
    • Koeppen AH, Dickson AC. Iron in the Hallervorden-Spatz syndrome. Pediatr Neurol 2001; 25: 148-155.
    • (2001) Pediatr. Neurol. , vol.25 , pp. 148-155
    • Koeppen, A.H.1    Dickson, A.C.2
  • 25
    • 0033953962 scopus 로고    scopus 로고
    • Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and Lewy body pathology
    • Wakabayashi K, Fukushima T, Koide R et al. Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and Lewy body pathology. Acta Neuropathol 2000; 99: 331-336.
    • (2000) Acta Neuropathol. , vol.99 , pp. 331-336
    • Wakabayashi, K.1    Fukushima, T.2    Koide, R.3
  • 26
    • 0027489477 scopus 로고
    • A case of Hallervorden-Spatz syndrome with marked atrophy of the brainstem and cerebellum
    • Sodeyama N, Arai M, Sanjoh N, Orimo S, Tamaki M. A case of Hallervorden-Spatz syndrome with marked atrophy of the brainstem and cerebellum. Rinsho Shinkeigaku 1993; 33: 525-529.
    • (1993) Rinsho Shinkeigaku , vol.33 , pp. 525-529
    • Sodeyama, N.1    Arai, M.2    Sanjoh, N.3    Orimo, S.4    Tamaki, M.5
  • 28
    • 16144365391 scopus 로고    scopus 로고
    • Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p 12.3-p13
    • Taylor TD, Litt M, Kramer P et al. Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p 12.3-p13. Nature Genet 1996; 14: 479-481.
    • (1996) Nature Genet. , vol.14 , pp. 479-481
    • Taylor, T.D.1    Litt, M.2    Kramer, P.3
  • 29
    • 1642555537 scopus 로고    scopus 로고
    • Iron involvement in neural danage and microgliosis in models of neurodegenerative diseases
    • Shoham S, Youdim MBH. Iron involvement in neural danage and microgliosis in models of neurodegenerative diseases. Cell Mol Biol 2000; 46: 743-760.
    • (2000) Cell Mol. Biol. , vol.46 , pp. 743-760
    • Shoham, S.1    Youdim, M.B.H.2
  • 30
    • 0034851607 scopus 로고    scopus 로고
    • First scientific workshop on Hallervorden-Spatz syndrome: Executive summary
    • Hayflick SJ. First scientific workshop on Hallervorden-Spatz syndrome: Executive summary. Pediatr Neurol 2001; 25: 99-101.
    • (2001) Pediatr. Neurol. , vol.25 , pp. 99-101
    • Hayflick, S.J.1
  • 31
    • 0033709847 scopus 로고    scopus 로고
    • Friedreich's ataxia and iron metabolism
    • Gordon N. Friedreich's ataxia and iron metabolism. Brain Dev 2000; 22: 465-468.
    • (2000) Brain Dev. , vol.22 , pp. 465-468
    • Gordon, N.1
  • 32
    • 0035112680 scopus 로고    scopus 로고
    • Hereditary vitamin-E deficiency
    • Gordon N. Hereditary vitamin-E deficiency. Dev Med Child Neurol 2001; 43: 133-135.
    • (2001) Dev. Med. Child Neurol. , vol.43 , pp. 133-135
    • Gordon, N.1
  • 33
    • 0033817296 scopus 로고    scopus 로고
    • α-Synuclein accumulation in a case of neurodegeneration with brain iron accumulation type 1 (NBIA-1, formally Hallervorden-Spatz syndrome) with widespread cortical and brainstem-type Lewy bodies
    • Neumann M, Adler S, Schlüter O et al. α-Synuclein accumulation in a case of neurodegeneration with brain iron accumulation type 1 (NBIA-1, formally Hallervorden-Spatz syndrome) with widespread cortical and brainstem-type Lewy bodies. Acta Neuropathol 2000; 100: 568-574.
    • (2000) Acta Neuropathol. , vol.100 , pp. 568-574
    • Neumann, M.1    Adler, S.2    Schlüter, O.3
  • 34
    • 0033897735 scopus 로고    scopus 로고
    • Neurodegeneration with brain iron accumulation, type 1 is characterized by α- β-and γ-synuclein neuropathology
    • Galvin JE, Giasson B, Hurtig HI, Lee MV-Y, Trojanowski JQ. Neurodegeneration with brain iron accumulation, type 1 is characterized by α- β-and γ-synuclein neuropathology. Am J Pathol 2000; 157: 361-368.
    • (2000) Am. J. Pathol. , vol.157 , pp. 361-368
    • Galvin, J.E.1    Giasson, B.2    Hurtig, H.I.3    Lee, M.V.-Y.4    Trojanowski, J.Q.5
  • 35
    • 0029039795 scopus 로고
    • Time-dependent changes in iron levels and associated neuronal loss within the substantia nigra following lesions within the neostriatum/globus pallidus complex
    • Sastry S, Arendash GW. Time-dependent changes in iron levels and associated neuronal loss within the substantia nigra following lesions within the neostriatum/globus pallidus complex. Neuroscience 1995; 67: 649-666.
    • (1995) Neuroscience , vol.67 , pp. 649-666
    • Sastry, S.1    Arendash, G.W.2
  • 36
  • 37
  • 38
    • 0029589683 scopus 로고
    • Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy
    • Malandrini A, Cavallaro T, Fabrizi GM et al. Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. Virchows Arch 1995; 427: 415-421.
    • (1995) Virchows Arch. , vol.427 , pp. 415-421
    • Malandrini, A.1    Cavallaro, T.2    Fabrizi, G.M.3
  • 39
    • 0035964047 scopus 로고    scopus 로고
    • New genes reveal major role for iron in neurodegeneration
    • Senior K. New genes reveal major role for iron in neurodegeneration. Lancet 2001; 358: 302.
    • (2001) Lancet , vol.358 , pp. 302
    • Senior, K.1
  • 40
    • 0030908572 scopus 로고    scopus 로고
    • Hallervorden-Spatz disease: Late infantile type
    • Singhi P,Mitra S. Hallervorden-Spatz disease: late infantile type. J Child Neurol 1997; 12: 280-282.
    • (1997) J. Child Neurol. , vol.12 , pp. 280-282
    • Singhi, P.1    Mitra, S.2
  • 41
    • 0029939071 scopus 로고    scopus 로고
    • Continuous intrathecal baclofen infusion for symptomatic generalized dystonia
    • Albright AL, Barry MJ, Fasick P, Barron W, Shultz B. Continuous intrathecal baclofen infusion for symptomatic generalized dystonia. Neurosurgery 1996; 38: 934-939.
    • (1996) Neurosurgery , vol.38 , pp. 934-939
    • Albright, A.L.1    Barry, M.J.2    Fasick, P.3    Barron, W.4    Shultz, B.5
  • 42
    • 0031241013 scopus 로고    scopus 로고
    • Enfermedad de Hallervorden-Spatz y toxina botulinica
    • Diego MR, Garcia JN. Enfermedad de Hallervorden-Spatz y toxina botulinica. An Esp Pediatr 1997; 47: 443-444.
    • (1997) An. Esp. Pediatr. , vol.47 , pp. 443-444
    • Diego, M.R.1    Garcia, J.N.2
  • 43
    • 0013417021 scopus 로고    scopus 로고
    • Stereotactic pallidotomy in a child with Hallervorden-Spatz disease
    • Justesen CR, Penn RD, Kroin JS, Egel RT. Stereotactic pallidotomy in a child with Hallervorden-Spatz disease. J Neurosurg 90: 551-554.
    • J. Neurosurg. , vol.90 , pp. 551-554
    • Justesen, C.R.1    Penn, R.D.2    Kroin, J.S.3    Egel, R.T.4
  • 44
    • 0034125558 scopus 로고    scopus 로고
    • Anesthetic management for two-stage computer-assisted, stereotactic thalamotomy in a child with Hallervorden-Spatz disease
    • Keegan MT, Flick RP, Matsumoto JY, Davis DH, Lanier WL. Anesthetic management for two-stage computer-assisted, stereotactic thalamotomy in a child with Hallervorden-Spatz disease. J Neurosurg Anesthesiol 2000; 12: 107-111.
    • (2000) J. Neurosurg. Anesthesiol. , vol.12 , pp. 107-111
    • Keegan, M.T.1    Flick, R.P.2    Matsumoto, J.Y.3    Davis, D.H.4    Lanier, W.L.5
  • 45
    • 0035016293 scopus 로고    scopus 로고
    • Botulinium toxin for treatment of jaw opening dystonia in Hallervorden-Spatz syndrome
    • Dressler D, Wittstock M, Benecke R. Botulinium toxin for treatment of jaw opening dystonia in Hallervorden-Spatz syndrome. Eur Neurol 2001; 45: 287-288.
    • (2001) Eur. Neurol. , vol.45 , pp. 287-288
    • Dressler, D.1    Wittstock, M.2    Benecke, R.3
  • 46
    • 0034838767 scopus 로고    scopus 로고
    • Hallervorden-Spatz syndrome
    • Swaiman KF. Hallervorden-Spatz syndrome. Pediatr Neurol 2001; 25: 102-108.
    • (2001) Pediatr. Neurol. , vol.25 , pp. 102-108
    • Swaiman, K.F.1
  • 48
    • 0034851578 scopus 로고    scopus 로고
    • Iron overload, oxidative stress, and axonal dystrophy in brain disorders
    • Chiuch CC. Iron overload, oxidative stress, and axonal dystrophy in brain disorders. Pediatr Neurol 2001; 25: 138-147.
    • (2001) Pediatr. Neurol. , vol.25 , pp. 138-147
    • Chiuch, C.C.1


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