This is the first lecture about the anatomy of the brainstem discussing the definition of the brainstem and the anatomical relations along with the external and internal parts (in general) and listing the major functions of brainstem. Then describing the medulla oblongata with its location, external and internal functions at different levels of sections. Lastly, this lectures discusses the most important clinical syndromes affecting the medulla oblongata.
Here is anatomy and physiology of brain stem. Where we will discuss all three parts of brain stem. Starting from medulla, second is pons and third is mid brain. In this video I am presenting anatomy and physiology of medulla. Anatomy of medulla: Medulla Oblongata or more simply medulla is part of brain stem which forms base of the brain stem. Location of medulla oblongata is superior to spinal cord and inferior to Pons. It contains pyramid, olive and above pyramidal structure, there is decussation of pyramids which explains why each part of brain controls opposite part of body. Adding to that medulla also has several nuclei which controls activity of cardiovascular system and respiratory system. Medulla also has nuclei for controlling reflexes of vomiting, swallowing, hiccuping, coughing and sneezing. It has also nuclei for test, hearing and balance. Medulla also contains nuclei of cranial nerve number VIII, IX, X, XI and XII. Functions of medulla or what dose medulla do? So medulla controls blood pressure, diameter of wall of arteries, heart rate, basal respiration rate and also vomiting, swallowing, hiccuping, coughing and sneezing.
In this video, we explain you about anatomy and physiology of Pons. The reference material used to make video is: Principles of Anatomy and Physiology Gerard J. Tortora, Bryan H. Derrickson. Pons is part of brain stem, present superior to medulla, inferior to mid brain and anterior to cerebellum. Pons means a bridge. As the name denotes, it connects other areas of brain. Neurons extending from cerebral cortex to pons makes corticopontine tract. Pons is connected to cerebellum by middle cerebral peduncle. Pons has vestibular nuclei, which is part of equilibrium pathways from inner ear to brain. Pons has also respiratory nuclei. Along with rhythmicity area of medulla, pons controls basal respiratory rhythm. Pons also contains nuclei for cranial nerve number V, VI,VII, and VIII.
Neuroanatomy | 1. Introduction to NeuroanatomyAhmed Eljack
This is the first lecture in neuroanatomy presented and taught by Ahmed Eljack to second level medical students at Alneelain University.
This lecture discussed the basics of neuroanatomy regarding anatomical terms, planes of section, anatomical divisions of the nervous system, and cells of the nervous system and their major functions.
the fibers present in the cerebellar peduncles
the applied anatomy of the cerebellum
the microscopic structure of the cerebellum, mossy, and climbing fibers
Anatomy of thalamus,Nuclei of thalamus,functional classification of thalamic nuclei,afferent and efferent connections of thalamus,motor function of thalamus,alertness and arousal in thalamus,thalamus and emotional behavior,Thalamic syndrome,Korsakoff's Syndrome
This is the first lecture about the anatomy of the brainstem discussing the definition of the brainstem and the anatomical relations along with the external and internal parts (in general) and listing the major functions of brainstem. Then describing the medulla oblongata with its location, external and internal functions at different levels of sections. Lastly, this lectures discusses the most important clinical syndromes affecting the medulla oblongata.
Here is anatomy and physiology of brain stem. Where we will discuss all three parts of brain stem. Starting from medulla, second is pons and third is mid brain. In this video I am presenting anatomy and physiology of medulla. Anatomy of medulla: Medulla Oblongata or more simply medulla is part of brain stem which forms base of the brain stem. Location of medulla oblongata is superior to spinal cord and inferior to Pons. It contains pyramid, olive and above pyramidal structure, there is decussation of pyramids which explains why each part of brain controls opposite part of body. Adding to that medulla also has several nuclei which controls activity of cardiovascular system and respiratory system. Medulla also has nuclei for controlling reflexes of vomiting, swallowing, hiccuping, coughing and sneezing. It has also nuclei for test, hearing and balance. Medulla also contains nuclei of cranial nerve number VIII, IX, X, XI and XII. Functions of medulla or what dose medulla do? So medulla controls blood pressure, diameter of wall of arteries, heart rate, basal respiration rate and also vomiting, swallowing, hiccuping, coughing and sneezing.
In this video, we explain you about anatomy and physiology of Pons. The reference material used to make video is: Principles of Anatomy and Physiology Gerard J. Tortora, Bryan H. Derrickson. Pons is part of brain stem, present superior to medulla, inferior to mid brain and anterior to cerebellum. Pons means a bridge. As the name denotes, it connects other areas of brain. Neurons extending from cerebral cortex to pons makes corticopontine tract. Pons is connected to cerebellum by middle cerebral peduncle. Pons has vestibular nuclei, which is part of equilibrium pathways from inner ear to brain. Pons has also respiratory nuclei. Along with rhythmicity area of medulla, pons controls basal respiratory rhythm. Pons also contains nuclei for cranial nerve number V, VI,VII, and VIII.
Neuroanatomy | 1. Introduction to NeuroanatomyAhmed Eljack
This is the first lecture in neuroanatomy presented and taught by Ahmed Eljack to second level medical students at Alneelain University.
This lecture discussed the basics of neuroanatomy regarding anatomical terms, planes of section, anatomical divisions of the nervous system, and cells of the nervous system and their major functions.
the fibers present in the cerebellar peduncles
the applied anatomy of the cerebellum
the microscopic structure of the cerebellum, mossy, and climbing fibers
Anatomy of thalamus,Nuclei of thalamus,functional classification of thalamic nuclei,afferent and efferent connections of thalamus,motor function of thalamus,alertness and arousal in thalamus,thalamus and emotional behavior,Thalamic syndrome,Korsakoff's Syndrome
Thalamus which is the Relay center in our Body.
Anatomy & Physiology of Thalamus
Book references:- Snell's Anatomy and K. and prema Sembuligum
Medical
-Yash Bhandari (Physiotherapist)
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Adv. biopharm. APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMSAkankshaAshtankar
MIP 201T & MPH 202T
ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS : UNIT 5
APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMS By - AKANKSHA ASHTANKAR
share - Lions, tigers, AI and health misinformation, oh my!.pptxTina Purnat
• Pitfalls and pivots needed to use AI effectively in public health
• Evidence-based strategies to address health misinformation effectively
• Building trust with communities online and offline
• Equipping health professionals to address questions, concerns and health misinformation
• Assessing risk and mitigating harm from adverse health narratives in communities, health workforce and health system
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
DISSERTATION on NEW DRUG DISCOVERY AND DEVELOPMENT STAGES OF DRUG DISCOVERYNEHA GUPTA
The process of drug discovery and development is a complex and multi-step endeavor aimed at bringing new pharmaceutical drugs to market. It begins with identifying and validating a biological target, such as a protein, gene, or RNA, that is associated with a disease. This step involves understanding the target's role in the disease and confirming that modulating it can have therapeutic effects. The next stage, hit identification, employs high-throughput screening (HTS) and other methods to find compounds that interact with the target. Computational techniques may also be used to identify potential hits from large compound libraries.
Following hit identification, the hits are optimized to improve their efficacy, selectivity, and pharmacokinetic properties, resulting in lead compounds. These leads undergo further refinement to enhance their potency, reduce toxicity, and improve drug-like characteristics, creating drug candidates suitable for preclinical testing. In the preclinical development phase, drug candidates are tested in vitro (in cell cultures) and in vivo (in animal models) to evaluate their safety, efficacy, pharmacokinetics, and pharmacodynamics. Toxicology studies are conducted to assess potential risks.
Before clinical trials can begin, an Investigational New Drug (IND) application must be submitted to regulatory authorities. This application includes data from preclinical studies and plans for clinical trials. Clinical development involves human trials in three phases: Phase I tests the drug's safety and dosage in a small group of healthy volunteers, Phase II assesses the drug's efficacy and side effects in a larger group of patients with the target disease, and Phase III confirms the drug's efficacy and monitors adverse reactions in a large population, often compared to existing treatments.
After successful clinical trials, a New Drug Application (NDA) is submitted to regulatory authorities for approval, including all data from preclinical and clinical studies, as well as proposed labeling and manufacturing information. Regulatory authorities then review the NDA to ensure the drug is safe, effective, and of high quality, potentially requiring additional studies. Finally, after a drug is approved and marketed, it undergoes post-marketing surveillance, which includes continuous monitoring for long-term safety and effectiveness, pharmacovigilance, and reporting of any adverse effects.
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
12. • All sensory pathways relay in thalamus.
• Many circuits used by cerebellum, basal nuclei
and limbic system involve thalamus.
• These utilize more or less separate portions of
thalamus, which has been subdivided into a
series of nuclei.
13. • Nuclei can be distinguished from each other
by topographical locations within thalamus
and by input/output patterns.
• Thalamus is divided into medial and lateral
nuclear groups by a thin curved sheet of
myelinated fibres called internal medullary
lamina..
14. • It splits anteriorly to enclose a group of nuclei,
collectively called anterior nucleus, which is
close to interventricular foramen
• Medial group contains one large nucleus
called dosomedial nucleus
• Lateral group is subdivided into a dorsal and
ventral tier
15.
16.
17. • Dorsal tier consists of lateral dorsal, lateral
posterior nuclei and pulvinar.
• Lateral posterior nucleus and pulvinar have
almost similar connections
18. Nuclei of ventral tier
• Ventral anterior, ventral lateral- concerned
with motor control; are connected to basal
nuclei and cerebellum
• Ventral posterior is subdivided into ventral
posterolateral[ smatosensory input from
body] and ventral posteromedial
[somatosensory input from head]
19. • Lateral and medial geniculate nuclei / bodies
are considered as posterior extensions of
ventral tier
Intralaminar nuclei
• Embedded in internal medullary lamina
• Largest of this group are centromedian and
parafascicular nuclei
20. Reticular nucleus
• Lies between lateral thalamic surface and
external medullary lamina
• Reticular nucleus is developmentally not a
part of thalamus.
• It has distinct anatomical and physiological
properties.
• Considered a part of thalamus because of
location and extensive involvement in
thalamic function.
21. Midline nuclei
• Rostral continuation of periaqueductal gray
matter
• Form interthalamic adhesion [when present]
22. Role of thalamic nuclei
• Pipelines for flow of information to cerebral
cortex
• Site where decisions are implemented about
which information should reach cerebral
cortex for processing
• Any particular type of information affected by
any thalamic nucleus is a function of its input
and output connections
23. Inputs
• Specific - Regulatory
• Specific inputs convey information that a
given nucleus may pass to cerebral cortex
[and for some nuclei to additional sites].
• Examples; Medial lemniscus specifically to
VPL. Optic tract to LGB
24. • Regulatory inputs contribute to decisions
about whether or in what form information
leaves a thalamic nucleus
25.
26. Sources
• cortical area to which the nucleus projects
• thalamic reticular nucleus
• diffuse cholinergic, noradrenergic,
serotonergic endings from brainstem reticular
formation
27. Categories of nuclei depending on pattern of
inputs
Relay nuclei
• receive well defined specific input fibres and
project to specific functional areas of cerebral
cortex
• deliver information from specific functional
systems to appropriate cortical areas
Intralaminar and midline nuclei seem to have
special role in function of basal nuclei and
limbic system
28. Association nuclei
• project to association areas of cerebral cortex
• receive major inputs from cerebral cortex and
subcortical structures
• probably important in distribution and gating
of information between cortical areas
29. SCHEME OF THALAMIC ORGANIZATION
• Every nucleus of the thalamus except the
reticular nucleus sends axons to the cerebral
cortex, either to a sharply defined area or
diffusely to a large area.
• Every part of the cortex receives afferent
fibers from the thalamus, probably from at
least two nuclei.
30. • Every thalamocortical projection is faithfully
copied by a reciprocal corticothalamic
connection.
• Thalamic nuclei receive other afferent fibers
from subcortical regions.
• Probably only one noncortical structure, the
striatum , receives afferent fibers from the
thalamus.
• .
31. • The thalamocortical and corticothalamic
axons give collateral branches to neurons in
the reticular nucleus, whose neurons project
to and inhibit the other nuclei of the thalamus
• No connections exist between the various
nuclei of the main mass of the thalamus,
although each individual nucleus contains
interneurons
32. • The synapses of the interneurons are
inhibitory, and most are dendrodendritic.
• Other synapses in the thalamus are excitatory,
with glutamate as the transmitter, and so are
thalamocortical projections
36. RETICULAR NUCLEUS
Input Output Functions
Collateral branches To each thalamic Inhibitory
of thalamocortical nucleus that sends modulation of
and corticothalamic afferents to thalamocortical
axons reticular nucleus transmission
37. Intralaminar nuclei
Input Output Functions
Cholinergic and Extensive cortical Stimulation of
central nuclei of projections, cerebral cortex in
reticular especially to frontal waking state and
formation,locus and parietal lobes; arousal from
coeruleus, collateral striatum sleep;somatic
branches from sensation, especially
spinothalamictracts, pain [from
cerebellar nuclei, contralateral head
pallidum and body]; control
of movement
39. Medial geniculate body
Input Output Functions
Inferior colliculus Primary auditory Auditory pathway
cortex [from both ears]
40. Lateral geniculate body
Input Output Functions
Ipsilateral halves of Primary visual Visual pathway
both retinas cortex [from contralateral
visual fields]
41. Ventral posterolateral
Input Output Functions
Contralateral gracile Primary Somatic sensation
and cuneate nuclei; somatosensory area [principal pathway,
contralateral dorsal from contralateral
horn of spinal cord body below head]
42. Ventral posteromedial
Input Output Functions
Contralateral Primary Somatic sensation
trigeminal sensory somatosensory area [principal pathway,
nuclei from contralateral
side of head: face,
mouth, larynx,
pharynx, dura
mater]
43. Ventral lateral [posterior division]
Input Output Functions
Contralateral Primary motor area Cerebellar
cerebellar nuclei modulation of
commands sent to
motor neurons
44. Ventral lateral [anterior division]
Input Output Functions
Pallidum Premotor and Planning commands
supplementary to be sent to motor
motor areas neutons
45. Ventral anterior
Input Output Functions
Pallidum Frontal lobe, Motor planning and
including premotor more complex
and supplementary behavior
motor areas
46. Posterior group
Input Output Functions
Spinothalamic and Insula and nearby Visceral and other
trigeminothalamic temporal and responses to
tracts parietal cortex, somatic sensory
including second stimuli
somatosensory srea
48. Lateral dorsal
Input Output Functions
Hippocampal Cingulate gyrus; Memory ;
formation; pretectal visual association interpretation of
area, superior cortex visual stimuli
colliculus [occipital,posterior
parietal and
temporal lobes]
49. Lateral posterior
Input Output Functions
Superior colliculus Parietal, temporal, Interpretation of
and association visual and other
cortex sensory stimuli;
formation of
complex behavioral
responses
50. Pulvinar
Input Output Functions
Pretectal area; Parietal lobe, Interpretation of
primary and all anterior frontal visual and other
association cortex cortex, cingulate sensory stimuli,
for vision;retinas gyrus, amygdala formation of
complex behavioral
responses
52. Mediodorsal/dorsomedial
Input Output Functions
Etorhinal cortex, Prefrontal cortex Behavioral
amygdala responses that
,collaterals from involve decisions
spinothalamic tract, based on prediction
pallidum, substantia and incentives
nigra
53. ‘Midline’ nuclei
Input Output Funtions
Amygdala, Hippocampal Behaviorr;including
hypothalamus formation and visceral and
parahippocampal emotional
gyrus responses
54. Anterior
Input Output Funtions
Mamillary body Cingulate gyrus Memory
55.
56. Thalamic damage
• Vascular accidents
• Can involve adjacent structures
• Small lesion can lead to large collection of
deficits
57. Damage restricted to posterior
thalamus
• Paroxysms of intense pain triggered by
somatosensory stimuli
• Pain may spread to involve entire one- half of
the body- analgesic resistant
• Abnormal perception of stimuli that do not
cause pain
58. • Intensity and modality may be distorted
• May seem unusually uncomfortable or
unpleaseant
• Similar syndrome can develop in some
patients after damage in almost any part of
Anterolateral pathway
59. • This type of pain is called Thalamic
pain/central pain
• Cause not understood
• Lesions causing this pain always involve
VPL/VPM nuclei with sparing of spinothalamic
and spinoreticulothalamic fibres that end in
other thalamic nuclei
• May result in imbalanced thalamic activity
60. Extensive thalamic damage to
posterior thalamus
• Total/nearly total loss of somatic sensation in
contralateral head and body
• Gradually – return of some appreciation of
painful, thermal and gross tactile stimuli
• Functions associated with Medial lemniscus
tend to more severely and oermanently
impaired
61. • Discriminative touch may be abolished
• Position sense may be greatly impaired
• Sensory ataxia [due to loss of proprioception]
may be present
62. • Tahalamic pain+ hemianaesthesia+sensory
ataxia contralateral to a posterior thalamic
lesion= thalamic syndrome
• It is often accompanied by mild and transient
paralysis [damage to corticospinal fibres in
Internal capsule] and various types of
residual involuntary movements [damage to
adjacent basal nuclei]
63. It is often accompanied by
• mild and transient paralysis [damage to
corticospinal fibres in Internal capsule]
• various types of residual involuntary
movements [damage to adjacent basal
nuclei]