Abstract
The role of the cerebellum is to integrate the sensory input from the periphery to provide smooth coordinated voluntary movements. It is a laminated cortical region with four deep nuclei (dentate, fastifigial, emboliform, and interpositus) and is attached to the brain stem by three peduncles- the superior, middle and inferior cerebellar peduncles. Superior cerebellar peduncle (brachium conjunctivum) is primarily efferent and projects via the dentate, fastigial, and interpositus nucleus to the red nucleus of the midbrain and onto thalamic motor nuclei which then project onto cerebrum. The middle cerebellar peduncle (brachium pontis) is the largest cerebellar peduncle and receives input primarily from the contralateral cerebrum via deep pontine nuclei whose fibers then project onto the neocerebellum. The inferior cerebellar peduncle provides sensory input via climbing fibers from the inferior olivary nucleus of the medulla and proprioceptive mossy fibers from the spinocerebellar tract and lateral cuneate nucleus and projects onto the paleocerebellum. The juxtarestiform body lies next to the inferior cerebellar peduncle and carries ipsilateral input from the vestibular nuclei onto the flocculonodular lobe of the archicerebellum and midline vermis which are important in posture and movements.
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Notes
- 1.
However, the mossy fibers from the pontine and brain stem reticular nuclei apparently do not serve this collateral excitatory function.
- 2.
Medulloblastomas may occasionally occur in adolescents and young adults.
- 3.
Progressive multiple sclerosis may produce in the young or middle-aged adult severe involvement of white matter in the cerebellum and brain stem, resulting in severe truncal ataxia, in which the patient is ataxic in both the sitting and standing positions. Such cases almost always also manifest severe appendicular involvement, that is, the cerebellar syndrome is not selective.
- 4.
In general chronic lesions of cerebellum in humans do not alter tone or tendon reflexes. Acute lesions of cerebellum resulting from hemorrhage or surgery may produce transient hypotonia (Diener and Dichgans 1992).
- 5.
*As of April 2016, the number of identified loci has grown to 17. SCA 17 involves a CAG trinucleotide expansion.
Bibliography
Allin M, Matsumoto H, Santhouse AM, Nosarti C, et al. Cognitive and motor function and the size of the cerebellum in adolescents born very preterm. Brain. 2001;124:60–6.
Amarenco P, Chevrie-Muller C, Roullet E, Bousser MG. Paravermal infarct and isolated cerebellar dysarthria. Ann Neurol. 1991a;30:211–3.
Carrera RME, Mettler FA. Physiologic consequences following extensive removals of cerebellar cortex and deep cerebellar nuclei and effect of secondary cerebral ablations in the primate. J Comp Neurol. 1947;87:167–288.
Courchesne E, Townsend J, Saitoh O. The brain in infantile autism: posterior fossa structures are abnormal. Neurology. 1994;44:214–23.
Diener HC, Dichgans J. Pathophysiology of cerebellar ataxias. Mov Disord. 1992;7:95–109.
Dow RS, Moruzzi G. The physiology and pathology of the cerebellum. Minneapolis: University of Minnesota Press; 1958.
Drepper J, Timmann D, Kolb FP, Diener HC. Non-motor associative learning inpatients with isolated degenerative cerebellar disease. Brain. 1999;122:87–97.
Fiez JA, Petersen SE, Cheney MK, Raichle ME. Impaired non-motor learning and error detection associated with cerebellar damage. A single case study. Brain. 1992;115:155–78.
Gilman S. Cerebellum and motor function. In: Asbury AK, McKhann GM, Mc Donald WI, editors. Diseases of the nervous system clinical neurobiology, vol. 1. Philadelphia: W.B. Saunders; 1986. p. 401–22.
Holmes G. Clinical symptoms of cerebellar disease and their interpretation. The Croonian lectures. Lancet. 1922;1. 1177–1182, 1231–1237; 2:59–65, 111–115
Holmes G. The cerebellum of man. Brain. 1939;62:1–30.
Ito M. The cerebellum and motor control. New York: Raven Press; 1984.
Lechtenberg R. Ataxia and other cerebellar syndromes. In: Ankovic J, Tolosa E, editors. Parkinson’s disease and movement disorders. Baltimore/Munich: Urban & Schwarzenberg; 1988. p. 365–76.
Lechtenberg R, Gilman S. Speech disorders in cerebellar disease. Ann Neurol. 1978;3:285–90.
Levinsohn L, Cronin-Golomb A, Schmahmann JD. Neuropsychological consequences of cerebellar tumor resection in children. Brain. 2000;123:1041–50.
Mettler FA, Orioli F. Studies on abnormal movement: cerebellar ataxia. Neurology. 1958;8:953–61.
Noback, C.R. et al.: 1991. The Human Nervous System. 4th ed, Philadelphia. Lea & Febiger p. 282.
Orioli FL, Mettler FA. Consequences of section of the simian restiform body. J Comp Neurol. 1958;109:195–204.
Raymond JLS, Lisberger G, Mauk MD. The cerebellum: a neuronal learning machine? Science. 1996;272:1126–31.
Riva D, Giogi C. The cerebellum contributes to higher functions during development. Brain. 2000;123:10411061.
Sanes JN, Dimitrov B, Hallett M. Motor learning in patients with cerebellar dysfunction. Brain. 1990;113:103–20.
Schmahmann JD, Sherman JC. The cerebellar cognitive affective syndrome. Brain. 1998;121:561–79.
Snider. R.S.: 1950. Arch. Neurol. Psych. 64:204 (AMA).
Thach WT. Cerebellar inputs to motor cortex. In: Ciba foundation symposium 132: motor areas of the cerebral cortex. Chichester: John Wiley; 1987. p. 201–20.
Thach WT, Goodkin M, Keating JG. The cerebellum: the adaptive coordination of movement. Ann Rev Neurosci. 1992;15:402–42.
Topka H, Valls-Sole J, Massaquoi SG, Hallett M. Deficit in classical conditioning in patients with cerebellar degeneration. Brain. 1993;116:961–9.
Wood NW, Harding AE. Cerebellar and spinocerebellar disorders. In: Bradley WG, Daroff RB, Fenichel GM, Marsden CD, editors. Neurology in clinical practice, vol. II. Boston: Butterworth Heinemann; 2000b. p. 1931–51.
Cerebellum Degenerations and Systemic Disorders
Baloh RW, Yee RD, Honrubia V. Late cortical cerebellar atrophy: clinical and oculographic features. Brain. 1986;109:159–80.
Berciano J. Olivopontocerebellar atrophy. In: Jankovic J, Tolosa E, editors. Parkinson’s disease and movement disorders. Baltimore/Munich: Urban & Schwarzenberg; 1988. p. 131–51.
Bhatia KP, Griggs RC, Ptacek LJ. Episodic movement disorders as channelopathies. Mov Disord. 2000;15:429–33.
Burk K, Abele M, Fetter M, et al. Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA 1, SCA 2 and SCA 3. Brain. 1996;119:1497–505.
Fujigasaki H, Verma IC, Camuzat A, et al. SCA 12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family. Ann Neurol. 2001;49:117–21.
Giunti P, Sabbadini G,. Sweeney G,MG, et al. The role of the SCA 2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia. Frequency, clinical and genetic correlates. Brain. 1998;121:459–67.
Giunti P, Sweeney MG, Harding AE. Detection of the Machado-Joseph disease/spinocerebellar ataxia three trinucleotides repeat expansion in families with autosomal dominant motor disorders including the drew family of walworth. Brain. 1995;118:1077–85.
Greenfield JG. The spinocerebellar degenerations. Springfield, IL: Charles C Thomas; 1954.
Thomas CC, Harding AE. Friedreich’s ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intra-familial clustering of clinical features. Brain. 1981;104:589–620.
Klockgether T, Wullner U, Spauschus A, Evert B. The molecular biology of the autosomal- dominant cerebellar ataxias. Mov Disord. 2000;15:604–12.
Mason WP, Graus F, Lang B, et al. Small cell lung cancer, paraneoplastic cerebellar degeneration and the Lambert–Eaton myasthenia syndrome. Brain. 1997;120:1279–300.
Rosen FS, Harris NL. A 30-year-old man with ataxia telangiectasia and dysarthria. Case records of the Massachusetts General Hospital: Case #2–1987. N Engl J Med. 1987;316:91–100.
Rosenberg RN. Machado-Joseph disease: an autosomal dominant motor system degeneration. Mov Disord. 1992;7:193–203.
Rosenberg RN. DNA-triplet repeats and neurologic disease. N Engl J Med. 1996;335:1222–4.
Smitt PS, Kinoshita A, De Leeuw B, et al. Paraneoplastic cerebellar ataxia due to autoantibodies against a glutamate receptor. N Engl J Med. 2000;342:21–7.
Sudarsky L, Corwin L, Dawson DM. Machado-Joseph disease in New England: clinical description and distinction from olivopontocerebellar atrophy. Mov Disord. 1992;7:204–8.
Swift M, Morrell D, Massey RB, Chase CL. Incidence of cancer in 161 families affected by ataxia-telangiectasia. N Engl J Med. 1991;325:1831–6.
Tolosa E, Berciano J. Choreas, hereditary and other ataxias and other movement disorders. Curr Opin Neurol Neurosurg. 1993;6:358–68.
Truman JT, Richardson EP Jr, Dvorak HF. Case records of the Massachusetts General Hospital, case 22-1975 (Ataxia-Telangiectasia). N Engl J Med. 1975;292:1231–7.
Victor M, Adams RD, Collins GH. The Wernicke Korsakoff syndrome and related neurological disorders due to alcoholism and malnutrition. 2nd ed. F. A. Davis: Philadelphia; 1989.
Victor M, Adams RD, Mancall EL. A restricted form of cerebellar cortical degeneration occurring in alcoholic patients. Arch Neurol. 1959;1:579–688.
Yount WJ. IgG2 deficiency and ataxia telangiectas (editorial). N Engl J Med. 1981;306:541–3.
Vascular Syndromes of the Cerebellum
Amarenco P. The spectrum of cerebellar infarctions. Neurology. 1991;41:973–9.
Amarenco P, Hauw JJ. Cerebellar infarction in the territory of the superior cerebellar artery: a clinicopathologic study of 33 cases. Neurology. 1990a;40:1383–90.
Amarenco P, Hauw JJ. Cerebellar infarction in the territory of the anterior and inferior cerebellar artery. Brain. 1990b;113:139–55.
Amarenco P, Kase CS, Rosengart A, et al. Very small (border zone) cerebellar infarcts. Distribution, causes, mechanisms and clinical features. Brain. 1993;116:161–86.
Amarenco P, Roulellet E, Goujon C, et al. Infarction in the anterior rostral cerebellum (the territory of the lateral branch of the superior cerebellar artery). Neurology. 1991b;41:253–8.
Caplan LR. Vertebrobasilar occlusive disease. In: Barnett HJM, et al., editors. Stroke: pathophysiology diagnosis and management, vol. 1; 1986. p. 549–619.
Chaves CJ, Caplan LR, Chung CS, Amarenco P. Cerebellar infarcts. Curr Neurol. 1994;14:143–77.
Chaves C, Pessin MS, Caplan LR, et al. Cerebellar hemorrhagic infarction. Neurology. 1996;46:346–9.
Greenberg J, Skubick D, Shenkin H. Acute hydrocephalus in cerebellar infarct and hemorrhage. Neurology. 1979;29:409–13.
Heros R. Cerebellar infarction and hemorrhage. Stroke. 1982;13:106.
Kase CS, Caplan LR. Hemorrhage affecting the brain stem and cerebellum. In: Barnett HJM, et al., editors. Stroke: pathophysiology diagnosis and management, vol. 1; 1986. p. 621–41.
Kase CSB, Norrving O, Levine SR, et al. Cerebellar infarction. Clinical and anatomical observations in 66 patients. Stroke. 1993;24:76–83.
Skenkin HA, Zavala M. Cerebellar strokes: mortality, surgical indications and results of ventricular drainage. Lancet. 1982;11:429–31.
St. Louis EK, Wijdicks EF, Li H. Predicting neurologic deterioration in patients with cerebellar hematomas. Neurology. 1998;51:1364–9.
Sypert GW, Alvord EC. Cerebellar infarction. A clinicopathological study. Arch Neurol. 1975;32:357–63.
Cerebellum and Tremor
Colebatch JG, Britton T, Findley LJ, et al. The cerebellum is activated in essential tremor. Lancet. 1990;2:1028–30.
Deuschl G. Tremor: basic mechanisms and clinical aspects. Mov Disord. 1998;13(Suppl 3):1–149.
Deuschl G, Wenzelburger R, Loffler K, et al. Essential tremor and cerebellar dysfunction. Clinical and kinematic analysis of intention tremor. Brain. 2000;123:1568–80.
Dupuis MJM, Delwaide PJ, Boucguey D, Gonette RE. Homolateral disappearance of essential tremor after cerebellar stroke. Mov Disord. 1989;4:183–7.
Elble RJ. Animal models of action tremor. Mov Disord. 1998;13(S3):35–9.
Findley LJ. Tremors: differential diagnosis and pharmacology. In: Jankovic J, Tolosa E, editors. Parkinson’s disease and movement disorders. Baltimore/Munich: Urban & Schwarzenberg; 1988. p. 243–61.
Hallett M. Classification and treatment of tremor. JAMA. 1991;266:1115–7.
Hallett M. Overview of human tremor physiology. Mov Disord. 1998;13(S3):43–8.
Hua S, Reich SG, Zirh AT, et al. The role of the thalamus and basal ganglia in Parkinsonian tremor. Mov Disord. 1998;13(S3):40–2.
Gait Disorders of the Elderly
Adams RD, Fisher CM, Hakim S, et al. Symptomatic occult hydrocephalus with “normal” cerebrospinal fluid pressure: a treatable syndrome. N Engl J Med. 1965;273:117–26.
Fisher CM. Hydrocephalus as a cause of disturbances of gait in the elderly. Neurology. 1982;32:1358–63.
Fishman RA. Normal pressure hydrocephalus and arthritis (editorial). N Engl J Med. 1985;312:1255–6.
Hachinski VC, Potter P, Merskey H. Leuko-araiosis. Arch Neurol. 1987;44:21–3.
Inzitar D, Diaz F, Fox A, et al. Vascular risk factors and leuko-araiosis. Arch Neurol. 1987;44:42–7.
Jacobs L, Conti D, Kinkel WR, Manning EJ. “Normal pressure” hydrocephalus: relationship of clinical and radiographic findings to improvement following shunt surgery. JAMA. 1976;235:510–2.
Masdeu JC, Wolfson L, Lantos G, et al. Brain white matter changes in the elderly prone to falling. Arch Neurol. 1989;46:1292–6.
Rasker JJ, Jansen ENH, Haan J, Oostrom J. Normal pressure hydrocephalus in rheumatic patients: a diagnostic pitfall. N Engl J Med. 1985;312:1239–41.
Steingart A, Hackinski VC, Lau C, et al. Cognitive and neurological findings in subjects with diffuse white matter changes on computed topographic scan (leukoariosis). Arch Neurol. 1987;44:32–4.
Sudarsky L. Current concepts-geriatrics: gait disorders in the elderly. N Engl J Med. 1990;322:1441–6.
Sudarsky L, Ronthal M. Gait disorders among elderly patients: a survey study of 50 patients. Arch Neurol. 1983;40:740–3.
Thompson PD, Marsden CD. Gait disorder of subcorttical arteriosclerotic encephalopathy: Binswanger’s disease. Mov Disord. 1987;2:1–8.
Tinetti MD, Speechly M. Current concepts: geriatrics: prevention of falls among the elderly. N Engl J Med. 1989;320:1055–9.
Tinetti MD, Speechly M, Ginter SF. Risk factors for falls among elderly persons living in the community. N Engl J Med. 1988;319:1701–7.
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Jacobson, S., Marcus, E.M., Pugsley, S. (2018). Motor Systems III: The Cerebellum Movement and Major Fiber Pathways of the Cerebellum. In: Neuroanatomy for the Neuroscientist. Springer, Cham. https://doi.org/10.1007/978-3-319-60187-8_13
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