Skip to main content Accessibility help
×
Hostname: page-component-8448b6f56d-xtgtn Total loading time: 0 Render date: 2024-04-23T13:00:26.840Z Has data issue: false hasContentIssue false

Chapter 9 - A Phenomenology-Based Approach to Inborn Errors of Metabolism with Parkinsonism

from Section I - General Principles and a Phenomenology-Based Approach to Movement Disorders and Inherited Metabolic Disorders

Published online by Cambridge University Press:  24 September 2020

Darius Ebrahimi-Fakhari
Affiliation:
Harvard Medical School
Phillip L. Pearl
Affiliation:
Harvard Medical School
Get access

Summary

Parkinsonism is a syndrome diagnosed by the presence of cardinal motor features, generally defined as bradykinesia in combination with rigidity, resting tremor, flexed (stooped) posture, and freezing and/or impaired postural reflexes [1, 2]. Bradykinesia, the hallmark feature, is determined by the presence of the “sequence effect” (also known as fatiguing or decrement): repetition leads to progressive decrease in speed and/or amplitude of movements [3]. Hypokinesia describes a small amplitude of movements (with or without fatigue) and akinesia literally means “lack of movement.” Hypokinesia is sometimes equated to parkinsonism (as in “infantile hypokinetic–rigid syndrome”), but technically is not the same phenomenon.

Type
Chapter
Information
Movement Disorders and Inherited Metabolic Disorders
Recognition, Understanding, Improving Outcomes
, pp. 124 - 142
Publisher: Cambridge University Press
Print publication year: 2020

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Fahn, S, Jankovic, J, Hallett, M. Principles and Practice of Movement Disorders, 2nd edn. Philadelphia, PA: Elsevier; 2011.Google Scholar
Postuma, RB, Berg, D, Stern, M, et al. MDS clinical diagnostic criteria for Parkinson’s disease. Mov Disord. 2015;30(12):1591–601.Google Scholar
Kang, SY, Wasaka, T, Shamim, EA, et al. Characteristics of the sequence effect in Parkinson’s disease. Mov Disord. 2010;25(13):2148–55.Google Scholar
Golbe, LI. Young-onset Parkinson’s disease: A clinical review. Neurology. 1991;41(2(Pt 1)):168–73.Google Scholar
Quinn, N, Critchley, P, Marsden, CD. Young onset Parkinson’s disease. Mov Disord. 1987;2(2):7391.Google Scholar
Paviour, DC, Surtees, RA, Lees, AJ. Diagnostic considerations in juvenile parkinsonism. Mov Disord. 2004;19(2):123–35.Google Scholar
Correia Guedes, L, Ferreira, JJ, Rosa, MM, et al. Worldwide frequency of G2019S LRRK2 mutation in Parkinson’s disease: A systematic review. Parkinsonism Relat Disord. 2010;16(4):237–42.Google Scholar
Schneider, SA, Alcalay, RN. Neuropathology of genetic synucleinopathies with parkinsonism: Review of the literature. Mov Disord. 2017;32(11):1504–23.Google Scholar
Mandemakers, W, Quadri, M, Stamelou, M, Bonifati, V. TMEM230: How does it fit in the etiology and pathogenesis of Parkinson’s disease? Mov Disord. 2017;32(8):1159–62.CrossRefGoogle ScholarPubMed
Kumaran, R, Cookson, MR. Pathways to Parkinsonism redux: Convergent pathobiological mechanisms in genetics of Parkinson’s disease. Hum Mol Genet. 2015;24(R1):R3244.Google Scholar
Garcia-Cazorla, A, Duarte, ST. Parkinsonism and inborn errors of metabolism. J Inherit Metab Dis. 2014;37(4):627–42.CrossRefGoogle ScholarPubMed
Schrag, A, Schott, JM. Epidemiological, clinical, and genetic characteristics of early-onset parkinsonism. Lancet Neurol. 2006;5(4):355–63.Google Scholar
Fernandez-Alvarez, E. Frequency of movement disorders in children. Rev Neurol. 2001;33(3):228–9.Google Scholar
Fernandez-Alvarez, E, Aicardi, J. Movement Disorders in Children. London: Mac Keith Press; 2001.Google Scholar
Garcia-Cazorla, A, Ortez, C, Perez-Duenas, B, et al. Hypokinetic–rigid syndrome in children and inborn errors of metabolism. Eur J Paediatr Neurol. 2011;15(4):295302.Google Scholar
Kurian, MA, Gissen, P, Smith, M, Heales, S, Jr., Clayton, PT. The monoamine neurotransmitter disorders: An expanding range of neurological syndromes. Lancet Neurol. 2011;10(8):721–33.CrossRefGoogle ScholarPubMed
Ng, J, Papandreou, A, Heales, SJ, Kurian, MA. Monoamine neurotransmitter disorders: Clinical advances and future perspectives. Nat Rev Neurol. 2015;11(10):567–84.Google Scholar
Rodan, LH, Gibson, KM, Pearl, PL. Clinical use of CSF neurotransmitters. Pediatr Neurol. 2015;53(4):277–86.Google Scholar
Wijemanne, S, Jankovic, J. Dopa-responsive dystonia: Clinical and genetic heterogeneity. Nat Rev Neurol. 2015;11(7):414–24.Google Scholar
Rilstone, JJ, Alkhater, RA, Minassian, BA. Brain dopamine–serotonin vesicular transport disease and its treatment. N Engl J Med. 2013;368(6):543–50.CrossRefGoogle ScholarPubMed
Brun, L, Ngu, LH, Keng, WT, et al. Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency. Neurology. 2010;75(1):6471.Google Scholar
Segawa, M, Nomura, Y, Nishiyama, N. Autosomal dominant guanosine triphosphate cyclohydrolase I deficiency (Segawa disease). Ann Neurol. 2003;54 Suppl 6:S3245.Google Scholar
Furukawa, Y, Kish, SJ, Bebin, EM, et al. Dystonia with motor delay in compound heterozygotes for GTP-cyclohydrolase I gene mutations. Ann Neurol. 1998;44(1):10–6.Google Scholar
Opladen, T, Hoffmann, G, Horster, F, et al. Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia. Mov Disord. 2011;26(1):157–61.Google Scholar
Friedman, J, Roze, E, Abdenur, JE, et al. Sepiapterin reductase deficiency: A treatable mimic of cerebral palsy. Ann Neurol. 2012;71(4):520–30.Google Scholar
Opladen, T, Hoffmann, GF, Blau, N. An international survey of patients with tetrahydrobiopterin deficiencies presenting with hyperphenylalaninaemia. J Inherit Metab Dis. 2012;35(6):963–73.Google Scholar
Takahashi, Y, Manabe, Y, Nakano, Y, et al. Parkinsonism in association with dihydropteridine reductase deficiency. Case Rep Neurol. 2017;9(1):1721.Google Scholar
Willemsen, MA, Verbeek, MM, Kamsteeg, EJ, et al. Tyrosine hydroxylase deficiency: A treatable disorder of brain catecholamine biosynthesis. Brain. 2010;133(Pt 6):1810–22.Google Scholar
Hoffmann, GF, Assmann, B, Brautigam, C, et al. Tyrosine hydroxylase deficiency causes progressive encephalopathy and dopa-nonresponsive dystonia. Ann Neurol. 2003;54 Suppl 6:S5665.Google Scholar
Pons, R, Syrengelas, D, Youroukos, S, et al. Levodopa-induced dyskinesias in tyrosine hydroxylase deficiency. Mov Disord. 2013;28(8):1058–63.Google Scholar
Chien, YH, Lee, NC, Tseng, SH, et al. Efficacy and safety of AAV2 gene therapy in children with aromatic L-amino acid decarboxylase deficiency: An open-label, phase 1/2 trial. Lancet Child Adolesc Health. 2017;1(4):265–73.Google Scholar
Jacobsen, JC, Wilson, C, Cunningham, V, et al. Brain dopamine–serotonin vesicular transport disease presenting as a severe infantile hypotonic parkinsonian disorder. J Inherit Metab Dis. 2016;39(2):305–8.Google Scholar
Saito, T. Presenting symptoms and natural history of Wilson disease. Eur J Pediatr. 1987;146(3):261–5.Google Scholar
Czlonkowska, A, Litwin, T, Chabik, G. Wilson disease: Neurologic features. Handb Clin Neurol. 2017;142:101–19.Google Scholar
Machado, A, Chien, HF, Deguti, MM, et al. Neurological manifestations in Wilson’s disease: Report of 119 cases. Mov Disord. 2006;21(12):2192–6.Google Scholar
Hayflick, SJ, Kurian, MA, Hogarth, P. Neurodegeneration with brain iron accumulation. Handb Clin Neurol. 2018;147:293305.Google Scholar
Hogarth, P, Gregory, A, Kruer, MC, et al. New NBIA subtype: Genetic, clinical, pathologic, and radiographic features of MPAN. Neurology. 2013;80(3):268–75.Google Scholar
Hayflick, SJ, Kruer, MC, Gregory, A, et al. Beta-propeller protein-associated neurodegeneration: A new X-linked dominant disorder with brain iron accumulation. Brain. 2013;136(Pt 6):1708–17.Google Scholar
Costello, DJ, Walsh, SL, Harrington, HJ, Walsh, CH. Concurrent hereditary haemochromatosis and idiopathic Parkinson’s disease: A case report series. J Neurol Neurosurg Psychiatry. 2004;75(4):631–3.Google Scholar
Sedel, F, Saudubray, JM, Roze, E, Agid, Y, Vidailhet, M. Movement disorders and inborn errors of metabolism in adults: A diagnostic approach. J Inherit Metab Dis. 2008;31(3):308–18.Google Scholar
Marti-Sanchez, L, Ortigoza-Escobar, JD, Darling, A, et al. Hypermanganesemia due to mutations in SLC39A14: Further insights into Mn deposition in the central nervous system. Orphanet J Rare Dis. 2018;13:28.Google Scholar
Tuschl, K, Meyer, E, Valdivia, LE, et al. Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism–dystonia. Nat Commun. 2016;7:11601.Google Scholar
Tuschl, K, Clayton, PT, Gospe, SM, Jr., et al. Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man. Am J Hum Genet. 2016;99(2):521.Google Scholar
Ebrahimi-Fakhari, D, Hildebrandt, C, Davis, PE, et al. The spectrum of movement disorders in childhood-onset lysosomal storage diseases. Mov Disord Clin Pract. 2018;5(2):149–55.Google Scholar
Dehay, B, Martinez-Vicente, M, Caldwell, GA, et al. Lysosomal impairment in Parkinson’s disease. Mov Disord. 2013;28(6):725–32.Google Scholar
Liu, JP, Tang, Y, Zhou, S, et al. Cholesterol involvement in the pathogenesis of neurodegenerative diseases. Mol Cell Neurosci. 2010;43(1):3342.Google Scholar
Kraoua, I, Stirnemann, J, Ribeiro, MJ, et al. Parkinsonism in Gaucher’s disease type 1: Ten new cases and a review of the literature. Mov Disord. 2009;24(10):1524–30.Google Scholar
Hendriksz, CJ, Anheim, M, Bauer, P, et al. The hidden Niemann–Pick type C patient: Clinical niches for a rare inherited metabolic disease. Curr Med Res Opin. 2017;33(5):877–90.Google Scholar
Coleman, RJ, Robb, SA, Lake, BD, Brett, EM, Harding, AE. The diverse neurological features of Niemann–Pick disease type C: A report of two cases. Mov Disord. 1988;3(4):295–9.Google Scholar
Mole, SE, Williams, RE. Neuronal ceroid-lipofuscinoses. GeneReviews®. 2001;Oct 10 (updated Aug 1, 2013).Google Scholar
Bras, J, Verloes, A, Schneider, SA, Mole, SE, Guerreiro, RJ. Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis. Hum Mol Genet. 2012;21(12):2646–50.Google Scholar
Mink, JW, Augustine, EF, Adams, HR, Marshall, FJ, Kwon, JM. Classification and natural history of the neuronal ceroid lipofuscinoses. J Child Neurol. 2013;28(9):1101–5.Google Scholar
Behrens, MI, Bruggemann, N, Chana, P, et al. Clinical spectrum of Kufor–Rakeb syndrome in the Chilean kindred with ATP13A2 mutations. Mov Disord. 2010;25(12):1929–37.Google Scholar
Roze, E, Paschke, E, Lopez, N, et al. Dystonia and parkinsonism in GM1 type 3 gangliosidosis. Mov Disord. 2005;20(10):1366–9.Google Scholar
Gravel, RA, Kaback, MM, Proia, RL, et al. The GM2 gangliosidoses. In Beaudet, AL, Vogelstein, B, Kinzler, KW, et al., editors. The Online Metabolic and Molecular Bases of Inherited Disease. New York, NY: McGraw-Hill; 2014. [Online, accessed Dec 1, 2019;doi:10.1036/ommbid.184.]Google Scholar
Inzelberg, R, Korczyn, AD. Parkinsonism in adult-onset GM2 gangliosidosis. Mov Disord. 1994;9(3):375–7.Google Scholar
Silveira-Moriyama, L, Moriyama, TS, Gabbi, TV, Ranvaud, R, Barbosa, ER. Chédiak–Higashi syndrome with parkinsonism. Mov Disord. 2004;19(4):472–5.Google Scholar
Hara, M, Inokuchi, T, Taniwaki, T, et al. An adult patient with mucolipidosis III alpha/beta presenting with parkinsonism. Brain Dev. 2013;35(5):462–5.Google Scholar
Finsterer, J. Parkinson’s syndrome and Parkinson’s disease in mitochondrial disorders. Mov Disord. 2011;26(5):784–91.Google Scholar
Martikainen, MH, Ng, YS, Gorman, GS, et al. Clinical, genetic, and radiological features of extrapyramidal movement disorders in mitochondrial disease. JAMA Neurol. 2016;73(6):668–74.Google Scholar
Ghaoui, R, Sue, CM. Movement disorders in mitochondrial disease. J Neurol. 2018;265(5):1230–40.Google Scholar
Luoma, PT, Eerola, J, Ahola, S, et al. Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease. Neurology. 2007;69(11):1152–9.Google Scholar
Luoma, P, Melberg, A, Rinne, JO, et al. Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: Clinical and molecular genetic study. Lancet. 2004;364(9437):875–82.Google Scholar
Garcia-Cazorla, A, Rabier, D, Touati, G, et al. Pyruvate carboxylase deficiency: Metabolic characteristics and new neurological aspects. Ann Neurol. 2006;59(1):121–7.Google Scholar
Sakaue, S, Kasai, T, Mizuta, I, et al. Early-onset parkinsonism in a pedigree with phosphoglycerate kinase deficiency and a heterozygous carrier: Do PGK-1 mutations contribute to vulnerability to parkinsonism? NPJ Parkinsons Dis. 2017;3:13.Google Scholar
Sotiriou, E, Greene, P, Krishna, S, Hirano, M, DiMauro, S. Myopathy and parkinsonism in phosphoglycerate kinase deficiency. Muscle Nerve. 2010;41(5):707–10.Google Scholar
Pons, R, Collins, A, Rotstein, M, Engelstad, K, De Vivo, DC. The spectrum of movement disorders in Glut-1 deficiency. Mov Disord. 2010;25(3):275–81.Google Scholar
Tabarki, B, Al-Shafi, S, Al-Shahwan, S, et al. Biotin-responsive basal ganglia disease revisited: Clinical, radiologic, and genetic findings. Neurology. 2013;80(3):261–7.Google Scholar
Ozand, PT, Gascon, GG, Al Essa, M, et al. Biotin-responsive basal ganglia disease: A novel entity. Brain. 1998;121 (Pt 7):1267–79.Google Scholar
Kikuchi, K, Hamano, S, Mochizuki, H, Ichida, K, Ida, H. Molybdenum cofactor deficiency mimics cerebral palsy: Differentiating factors for diagnosis. Pediatr Neurol. 2012;47(2):147–9.Google Scholar
Alkufri, F, Harrower, T, Rahman, Y, et al. Molybdenum cofactor deficiency presenting with a parkinsonism–dystonia syndrome. Mov Disord. 2013;28(3):399401.Google Scholar
Nie, S, Chen, G, Cao, X, Zhang, Y. Cerebrotendinous xanthomatosis: A comprehensive review of pathogenesis, clinical manifestations, diagnosis, and management. Orphanet J Rare Dis. 2014;9:179.Google Scholar
Federico, A, Dotti, MT, Gallus, GN. Cerebrotendinous xanthomatosis. GeneReviews®. 2003; Jul 16 (updated Apr 14, 2016).Google Scholar
Su, CS, Chang, WN, Huang, SH, et al. Cerebrotendinous xanthomatosis patients with and without parkinsonism: Clinical characteristics and neuroimaging findings. Mov Disord. 2010;25(4):452–8.Google Scholar
Gitiaux, C, Roze, E, Kinugawa, K, et al. Spectrum of movement disorders associated with glutaric aciduria type 1: A study of 16 patients. Mov Disord. 2008;23(16):2392–7.Google Scholar
Gascon, GG, Ozand, PT, Brismar, J. Movement disorders in childhood organic acidurias. Clinical, neuroimaging, and biochemical correlations. Brain Dev. 1994;16 Suppl:94–103.Google Scholar
Sinclair, AJ, Barling, L, Nightingale, S. Recurrent dystonia in homocystinuria: A metabolic pathogenesis. Mov Disord. 2006;21(10):1780–2.Google Scholar
Ekinci, B, Apaydin, H, Vural, M, Ozekmekci, S. Two siblings with homocystinuria presenting with dystonia and parkinsonism. Mov Disord. 2004;19(8):962–4.Google Scholar
Ramos, EM, Carecchio, M, Lemos, R, et al. Primary brain calcification: An international study reporting novel variants and associated phenotypes. Eur J Hum Genet. 2018;26(10):1462–77.Google Scholar
Batla, A, Tai, XY, Schottlaender, L, et al. Deconstructing Fahr’s disease/syndrome of brain calcification in the era of new genes. Parkinsonism Relat Disord. 2017;37:110.Google Scholar
Manyam, BV, Walters, AS, Keller, IA, Ghobrial, M. Parkinsonism associated with autosomal dominant bilateral striopallidodentate calcinosis. Parkinsonism Relat Disord. 2001;7(4):289–95.CrossRefGoogle ScholarPubMed
Ramos, EM, Oliveira, JR, Sobrido, MJ, Coppola, G. Primary familial brain calcification. GeneReviews®. 2004;Apr 18 (updated Aug 24, 2017).Google Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×