File:Diseases of the nervous system - a text-book of neurology and psychiatry (1915) (14780493694).jpg

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Identifier: diseasesofnervo00jell (find matches)
Title: Diseases of the nervous system : a text-book of neurology and psychiatry
Year: 1915 (1910s)
Authors: Jelliffe, Smith Ely, 1866-1945 White, William A. (William Alanson), 1870-1937
Subjects: Mental Disorders Nervous System Diseases
Publisher: Philadelphia : Lea & Febiger
Contributing Library: Columbia University Libraries
Digitizing Sponsor: Open Knowledge Commons

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re study of cerebellarrepresentation will see marked advance in the near future. Mingazzinis grouping of the conditions is as follows: 1. Pure unilateral ageneses and atrophies. 2. Pure bilateral ageneses and atrophies. 3. Cerebellar atrophies associated with (a) Disease of the cerebrum.(6) Disease of the spinal cord. 1. Unilateral loss of a lateral (in old sense) lobe may be presentwithout any symptoms according to present developed modes oftesting. Few of these cases have been tested by more recent methods.In certain instances unilateral atrophy has been associated withepileptiform convulsions, or retropulsion, when the superficies of theaffected hemisphere is atrophic; if the atrophy involves a part of thevermis, slight motor signs, such as slowing of the gait, have beenobserved. 2. Pure Bilateral Agenesis.—In some of the cases reported no symp-toms have been observed (old cases). The commonest symptoms are 1 Monatsch. f. Neur. u. Psych., 1906, xviii, 76. 412 CEREBELLAR SYNDROMES
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Fig. 215.—Pontine middle syndrome. Lesion of the lateral part of the left pontinetegmentum, involving the nuclei of the trigeminus, the crossed secondary sensorypaths of the tegmentum, partially involving the superior cerebellar peduncle (Pes)and the median lemniscus (Rm), and not involving the anterior portion of the pons. On the right there is hemianesthesia of the extremities of the syringomyeKc type,above all for pain and temperature sense. On the left there is paralysis of the muscles of mastication (pterygoid, masseter,temporal) by lesion of the motor nucleus of the trigeminus. There is slight anesthesiain the trigeminus legion (sensory nucleus V) and choreo-athetoid movements of theextremities from involvement of the superior cerebellar peduncle. (Dejerine.) (SeeChart, No. 13, p. 392.) FRIEDREICHS ATAXIA 413 difficulty in standing and walking. The patient, in high grades ofatrophy or aplasia, is unable to stand, or sometimes even to sit; inthe milder grades the station is wob

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