Abstract
In this chapter, we review patients with very unusual movement disorders, including Wilson’s disease, neuronal brain iron degeneration, disorders on the borderland of epilepsy, unusual forms of parkinsonism, and benign paroxysmal disorders of infancy.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Czlonkowska A, Litwin T, Chabik G. Wilson disease: neurologic features. Handb Clin Neurol. 2017;142:101–19. https://doi.org/10.1016/B978-0-444-63625-6.00010-0.
Machado A, Chien HF, Deguti MM, Cancado E, Azevedo RS, Scaff M, et al. Neurological manifestations in Wilson’s disease: report of 119 cases. Mov Disord. 2006;21(12):2192–6. https://doi.org/10.1002/mds.21170.
Lorincz MT. Neurologic Wilson’s disease. Ann N Y Acad Sci. 2010;1184:173–87. https://doi.org/10.1111/j.1749-6632.2009.05109.x.
Chakor RT, Bharote H, Eklare N, Tamboli K. Unilateral rubral tremors in Wilson’s disease treated with dimercaprol. Ann Indian Acad Neurol. 2015;18(1):115–6. https://doi.org/10.4103/0972-2327.144286.
Wilson SAK. Progressive lenticular degeneration: a familial nervous disease associated with cirrhosis of the liver. Brain. 1912;34(4):295–507. https://doi.org/10.1093/brain/34.4.295.
Termsarasab P, Tanenbaum DR, Frucht SJ. The phenomenology and natural history of idiopathic lower cranial dystonia. J Clin Mov Disord. 2014;1:3. https://doi.org/10.1186/2054-7072-1-3.
Hogarth P. Neurodegeneration with brain iron accumulation: diagnosis and management. J Mov Disord. 2015;8(1):1–13. https://doi.org/10.14802/jmd.14034.
Midena E, Frizziero L, Parrozzani R. Eye signs of Wilson disease: on and beyond the surface. In: Kerkar N, Roberts EA, editors. Clinical and translational perspectives on Wilson disease. London: Academic Press; 2019. p. 227–35.
Irani SR, Michell AW, Lang B, Pettingill P, Waters P, Johnson MR, et al. Faciobrachial dystonic seizures precede Lgi1 antibody limbic encephalitis. Ann Neurol. 2011;69(5):892–900. https://doi.org/10.1002/ana.22307.
Ohta K, Obara K. Hemiparkinsonism with a discrete lacunar infarction in the contralateral substantia nigra. Mov Disord. 2006;21(1):124–5. https://doi.org/10.1002/mds.20747.
Cardoso F. Movement disorders in childhood. Parkinsonism Relat Disord. 2014;20(Suppl 1):S13–6. https://doi.org/10.1016/S1353-8020(13)70006-3.
Limphaibool N, Iwanowski P, Holstad MJV, Perkowska K. Parkinsonism in inherited metabolic disorders: key considerations and major features. Front Neurol. 2018;9:857. https://doi.org/10.3389/fneur.2018.00857.
Aberg L, Liewendahl K, Nikkinen P, Autti T, Rinne JO, Santavuori P. Decreased striatal dopamine transporter density in JNCL patients with parkinsonian symptoms. Neurology. 2000;54(5):1069–74. https://doi.org/10.1212/wnl.54.5.1069.
Ng J, Papandreou A, Heales SJ, Kurian MA. Monoamine neurotransmitter disorders–clinical advances and future perspectives. Nat Rev Neurol. 2015;11(10):567–84. https://doi.org/10.1038/nrneurol.2015.172.
Korenke GC, Christen HJ, Hyland K, Hunneman DH, Hanefeld F. Aromatic L-amino acid decarboxylase deficiency: an extrapyramidal movement disorder with oculogyric crises. Eur J Paediatr Neurol. 1997;1(2–3):67–71.
Pons R, Ford B, Chiriboga CA, Clayton PT, Hinton V, Hyland K, et al. Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosis. Neurology. 2004;62(7):1058–65. https://doi.org/10.1212/wnl.62.7.1058.
Hadjipanayis A, Efstathiou E, Neubauer D. Benign paroxysmal torticollis of infancy: an underdiagnosed condition. J Paediatr Child Health. 2015;51(7):674–8. https://doi.org/10.1111/jpc.12841.
Renne B, Rueckriegel S, Ramachandran S, Radic J, Steinbok P, Singhal A. Bobble-head doll syndrome: report of 2 cases and a review of the literature, with video documentation of the clinical phenomenon. J Neurosurg Pediatr. 2018;21(3):236–46. https://doi.org/10.3171/2017.9.PEDS16704.
Agarwal N, Raheja A. Bobblehead-doll syndrome. N Engl J Med. 2019;380(5):e5. https://doi.org/10.1056/NEJMicm1808747.
Mallants C, Casteels K. Practical approach to childhood masturbation–a review. Eur J Pediatr. 2008;167(10):1111–7. https://doi.org/10.1007/s00431-008-0766-2.
Author information
Authors and Affiliations
Corresponding author
Electronic Supplementary Material
In this chapter, we present a group of patients with very unusual movement disorders. These patients are rare enough that even a movement disorder clinician may encounter them very infrequently in a career. Four categories of disorders are reviewed: metal and ion deposits; disorders on the borderland of epilepsy; unusual forms of parkinsonism; and benign paroxysmal disorders of infancy (MP4 3144930 kb)
Notes
Notes
Notes
Rights and permissions
Copyright information
© 2020 Springer Nature Switzerland AG
About this chapter
Cite this chapter
Frucht, S.J., Termsarasab, P. (2020). Very Unusual Phenomenologies. In: Movement Disorders Phenomenology. Springer, Cham. https://doi.org/10.1007/978-3-030-36975-0_16
Download citation
DOI: https://doi.org/10.1007/978-3-030-36975-0_16
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-36974-3
Online ISBN: 978-3-030-36975-0
eBook Packages: MedicineMedicine (R0)