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THE CEREBRUM (Applied)
Dr. Md. Ziaul Hoque
MD Phase B Student
Department of Neurology
Outlines of discussion
• Radiological location of parts of cerebrum
• Lobe wise dysfunctions of cerebrum
• The disconnection syndrome
• Disorders of the cerebrum
• Disorder of speech and language
• Memory disturbance
Dominance & Handedness
Left Cerebral
Hemisphere is
dominant in -
– 90-95% Right
handed person
– 60% Left handed
person
Dysfunction of different lobes of cerebrum
Dysfunction of Frontal Lobe
Unilateral Bilateral
Either right or left Dominant Both
Contralateral hemiplegia Right hemiplegia
Broca’s aphasia
Bilateral hemiplegia
Pseudobulbar palsy
Gaze palsy &
Head turning
Sympathetic apraxia of
left hand
Gait apraxia
Sphincter incontinence
Apathy,
Loss of initiative
Elevation of mood,
Increased talkativeness
etc.
Abulia or
Akinetic mutism
Rigidity of thinking etc
Anosmia Frontal release sign.
Dysfunction of Parietal Lobe
Either right or left Dominant Nondominant
Contralateral
hemisensory loss
(Hemianaesthesia)
Bilateral Ideational apaxia Visuospatial disorder
Bilateral Ideomotor apaxia Topographic memory loss
Contralateral
homonymous inferior
quadrantanopia
Alexia without agraphia
(pure word blindness)
Constructional apraxia
Dressing apraxia
Contralateral
Hemineglect
Gerstman syndrome
• Acalculia
• Agraphia
• Right left confusion
• Finger agnosia
Anosognosia
Visual inattention Astereognosis/ Tactile
agnosia
Confusion
Agraphesthesia
PARIETAL LOBE DYSFUNCTIONS
• DOMINANT HEMISPHERE:
 Gerstmann’s syndrome

Inferior parietal lobule
Tetrad of-
Finger agnosia
Rt.-Lt.confusion
Acalculia
Agraphia
Dysfunction of Temporal Lobe
Unilateral Bilateral
Either Rt or left Dominant Nondominant Both
Contralateral
homonymous superior
quadrantanopia
Wernicke’s
aphasia
Inabilty to
judge spatial
relationship
Amnesia
(Korsakoff
amnesic defect)
Seizure Nominal/anomic
aphasia
Amusia Cortical deafness
Deafness
Auditory, visual,
olfactory and gustatory
hallucination
Pure word
deafness/auditory
verbal agnosia
Agnosia for
sound
Apathy
Delirium-confusional
state
Kluver Bucy
syndrome
Emotional and
behavioral change
Disturbance of time
perception
Dysfunction of Occipital Lobe
Unilateral Bilateral
Either Rt or left Dominant Nondominant Both
Contralateral
congruent
homonymous
hemianopia
Alexia
without
agraphia
Visual illusion/
Metamorphosia
Cortical
blindness
Anton
syndrome
Elementary/
unformed
hallucination
Visual
object
agnosia
Visual
halllucination
Balint
syndrome
Hemichromatopsia Loss of
topographic
memory &
visual
orientation
Prosopragnosia
Achromatopsia
Clinical Scenario
A 60-years-old diabetic & hypertensive male
Presented with sudden onset of bilateral visual loss.
On examination :
Visual acuity - Reduced to hand movement on both eyes.
Fundoscopy - Normal on both side.
Both direct and consensual light reflex was present bilaterally.
OCCIPITAL LOBE DYSFUNCTIONS
BILATERAL OCCIPITAL DISEASE:
Cortical
blindness
OCCIPITAL LOBE DYSFUNCTIONS
 Anton’s syndrome
 Baliant’s syndrome
 Achromatopsia
Antons syndrome
• Denial of blindness
• Patients act as though they could see
• Collide with object on attempting to walk
• Offer excuse for the difficulties
Lesion extends beyond the striate cortex to involve the visual
association areas.
Clinical Scenario
A 50-year-old hypertensive male presented with history of
• Difficulty in seeing objects for last 2 weeks
• Required assistance for daily activities…
On examination:
• He had severe difficulty in
– pursuit eye movement on both side and
– reaching out to objects held by the examiner.
• He could recognize a key & a pen individually,
but failed to identify them when presented
simultaneously .
Balint syndrome
. A triad of -
(1) Optic ataxia
(2) Oculomotor apraxia
(3) Simultanagnosia.
Cause : Stroke involving bilateral parieto-occipital area of
brain (border zone between Brodmann area 7 & 19)
The Disconnection Syndrome
The Disconnection Syndrome
• Interregional connections of the cerebrum are required for
all natural sensory and motor functions.
• Lesions of the cerebral connecting pathways are known
as Disconnection syndrome.
• Two types-
– Intrahemispheric
– Interhemispheric
Intrahemispheric Disconnection Syndrome
Conduction aphasia
– Fluent paraphasic speech
– Relatively preserved
comprehension
– Severely impaired repetition
Site of Lesion:
Arcuate fasciculus
Intra hemispheric Disconnection Syndrome (cont.)
• Pure word deafness :
Lesion in the left superior temporal gyrus
Interruption of connection between
the primary & association auditory cortex,
also with language network resulting-
• Impaired comprehension of spoken words
• Impaired repetition
• No hearing defect
• Nonverbal sound can be heard without difficulty
Interhemispheric Disconnection Syndrome
Alexia without agraphia
• Inability to read
• Color anomia & difficulty in copying
word may be present.
• No difficulty in repetition, writtng or
naming objects
Site of Lesion:
Splenium & dominant occipital lobe
Interhemispheric Disconnection Syndrome (cont.)
Lesion of the entire corpus callosum
• Unable to match an object held in one
hand with that in the other
• Unable to match objects seen in either
half of visual field
• Unable to name object held in left hand.
• Alexic in left visual field.
Congenital agenesis
of corpus callosum
Interhemispheric Disconnection Syndrome (cont.)
Lesion anterior part of
Corpus callosum
(posterior to genu but anterior
to spenium)
– Apraxia of the left sided
limbs.
DISORDERS OF CEREBRUM
DISORDERS OF CEREBRUM
Vascular diseases:
Ischaemia
Haemorrhage
Case scenario
A 77-year- old woman presented with the sudden
onset of left-sided weakness and
numbness.
On examination, in addition to the weakness and
sensory loss, she had a
left homonymous hemianopia and was unaware of
her deficits, denying that there was
anything wrong with her.
Her eyes were deviated to the right.
Diffusion-weighted sequences
Importantly, other diseases, such as active
multiple sclerosis (MS) lesions, abscesses, or
tumors such as primary CNS lymphoma can
also demonstrate restricted diffusion.
If there is corresponding hypointensity (referred
to as “drop-out”) on the apparent diffusion
coeffi cient (ADC) map, then the diagnosis is
confirmed in the appropriate clinical setting.
.
Ischaemic stroke
Haemorhagic stroke
Wake up stroke
DWI-FLAIR-mismatch was shown to identify patients
within 3–4.5 h with high specificity and positive
predicted value
PWI-DWI mismatch
Case scenario
A 76-year-old man with hypertension and
diabetes underwent a coronary bypass artery
graft that was complicated by severe blood
loss. When he awoke, he was unable to move
his proximal right arm and would not speak
unless he became upset.
Watershed strokes
Case scenario
A 65-year-old man presented with confusion
and cortical blindness. His blood pressure in
the emergency room (ER) was 231/180.
Case scenario
Posterior reversible encephalopathy syndrome
PRES
PRES Occurs in the setting of rapid,severe
increases in blood pressure
It presents with a combination of visual loss,
seizures,headaches, and altered mental status.
CNS Vasculitis
• Ischemic stroke is the most common CNS
presentation.
• However, patients may suffer from a wide range
of clinical presentations including hemorrhages,
meningitis, and cognitive dysfunction.
• Involvement of the extracranial vessels leads to
headaches, visual loss, jaw claudication, and
cranial tenderness.
• Systemic symptoms such as fever, weight loss,
and malaise
CNS Vasculitis
Case scenario
• A 30-year-old female presented with double
vision and ataxia.
Three years earlier she had an episode where
she lost vision in her left eye for two weeks.
On examination, she was mildly ataxic, with
brisk reflexes, and both horizontal and vertical
nystagmus.
DISORDERS OF CEREBRUM
Demyelinating
MS
Case scenario
• An 18-year-old boy presented with seizures
with altered level of consciousness. His
attendent also gives the h/o fever, headache ,
lethargy, myalgia , malaise, fever, and vomiting
for 7 days
ADEM
CASE SCENARIO
• A 25-year-old woman had repeated episodes
of the sudden onset of fear on unpleasant
odor. These were followed by her losing
consciousness for several minutes and making
bizarre lip-smacking movements.
CASE SCENARIO
CASE SCENARIO
• A 23-year-old female presented with a cluster
of seizures. She was otherwise healthy. She
had been acting oddly for the past two weeks.
She was thinking that her neighbors were
spying on her. She was found missing two days
prior to her presentation in the emergency
room. The patient was diaphoretic on exam
and appeared paranoid about hospital staff.
CASE SCENARIO
CASE SCENARIO
• A 30-years-male known case of VSD presented
with headaches and left-sided weakness.
CASE SCENARIO
CASE SCENARIO
• A 28-year-old man developed Headache
,vomiting , diplopia
O/E
There is left sided abducens nerve palsy with
bilateral Papilledema
CASE SCENARIO
Case scenario
• A 65-year-old woman presented with
personality changes, paranoia, and confusion
over the course of several months.
On exam, she had mild bilateral papilledema
and weakness of her legs.
Case scenario
Case scenario
• A 56-year-old man presented to the hospital
with a seizure. He had been complaining of
headaches for the past several months and
becoming “slow” as per family.
• He also noticed that he was “bumping into
things” for the past few months.
Case scenario
Case scenario
• A 67-year-old man presented with a partial
seizure with secondary generalization.
• His daughter said that he had been
increasingly confused over the past few
weeks.
• He has significant smoking history
Case scenario
DISORDERS OF CEREBRUM
Traumatic:
Contusion
Case scenario
A 72-year-old woman was brought in by her family.
The patient herself said that she felt well, but her
family said that she had been “forgetting
everything” recently.
For example, she would purchase the same
products at the grocery store, forgetting that
she had bought them only several days earlier.
She had also become paranoid, feeling that
someone was moving her glasses and wallet.
She had no awareness of her deficits.
DISORDERS OF CEREBRUM
Degenerative:
Alzheimer disease
Pick disease
Case scenario
• 50 years old male, presented with complaints
of forgetfulness, talking irrelevantly since last
18 months. Patient developed symptoms of
confusion, ataxia, and altered behaviour 2
years back, for which he was treated as a case
of encephalitis. He later progressed to show
symptoms of amnesia. Neurological
examination revealed MMSE 15/30 ,absent
deep tendon reflexes
Case scenario
• A 65-year-old man presented with rapid-onset
dementia.
• On exam, he knew his name, but not his age
or the location. He thought he was in his office
, though he had not worked in several months.
He hada profound startle response to any
unexpected noise..
Case scenario
• A 59-year-old woman presented with several
falls.
On examination, she had asymmetric rigidity
with a shuffling gait.
She also developed uncontrolled movements
of her left arm.
An 8-year-old boy presented with
progressive dementia, blindness, and
seizures.
DISORDERS OF CEREBRUM
Inborn error of metabolism:
Leukodystrophy
Canavan disease
Case scenario
• An 8-year-old boy presented with mental
retardation and seizures since infancy. He had
a large “port-wine stain” on his upper face on
the right side.
Case scenario
• An 8-year-old child with MR developed
intractable seizures and mental retardation.
• The patient had autistic features and language
delays, but no focal motor or sensory deficits.
Case scenario
DISORDERS OF CEREBRUM
Developmental Disorders:
Lissencephaly (Agyria)
Pachygyria/Polymicrogyria
Holoprocencephaly (lobar/alobar)
Agenesis of corpus callosum
Apraxia
A disorder in which an
attentive patient loss the
ability to execute previously
learned activities in the
absence of weakness, ataxia,
sensory loss or
extrapyramidal derangement
that would be adequate to
explain the deficit
– Ideomotor apraxia
– Ideational apraxia
– Oral buccal lingual
apraxia
– Gait apraxia
– Constructional
apraxia
– Dressing apraxia
Disorders of speech and language
Disorder of Language
Aphasia
Anomic aphasia
Conduction
Transcortical sensory
Wernicke
Transcortical motor
Broca
Mixed transcortical
Global
Aphasia
Fluency
Comprehension
Repetition
+
-
+
-
+
-
+
-
+
-
+
-
+
-
Aphasia
Type Fluency Comprehension Repetition Naming
Broca’s Impaired Preserved Impaired Impaired
Wernicke’s Preserved Impaired Impaired Impaired
Global Impaired Impaired Impaired Impaired
Transcortical
motor
Impaired Preserved Preserved Impaired
Transcortical
sensory
Preserved Impaired Preserved Impaired
Isolation Impaired Impaired Preserved Impaired
Conduction Preserved Relatively
Preserved
Impaired Impaired
Anomic/
nominal
Preserved Preserved Preserved Impaired
Memory and intellectual disorders
• Known as dementia
• Defined by involvement of multiple cognitive
domains (memory, intellect, personality,
affection &mood)
• Causes may be reversible or irreversible
• Manifested by several ways
• Assessed by MMSE
• Treatment according to aetiology
• Prognosis variable
Dementia
Reversible causes Irreversible causes
Hypothyriodism
Thiamine deficiency
Vitamin B12 deficiency
Normal pressure hydrocephalus
Subdural hematoma
Chronic infection
Brain tumor
Drug intoxication
Autoimmune encephalopathy
Alzheimer’s
Frontotemporal dementia
Vascular
Parkinson’s
Dementia with lewy bodies
Huntington’s
Leukoencephalopathies
THANK YOU

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THE CEREBRUM -Applied Dr zia.pptx

  • 1. THE CEREBRUM (Applied) Dr. Md. Ziaul Hoque MD Phase B Student Department of Neurology
  • 2. Outlines of discussion • Radiological location of parts of cerebrum • Lobe wise dysfunctions of cerebrum • The disconnection syndrome • Disorders of the cerebrum • Disorder of speech and language • Memory disturbance
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  • 5. Dominance & Handedness Left Cerebral Hemisphere is dominant in - – 90-95% Right handed person – 60% Left handed person
  • 6. Dysfunction of different lobes of cerebrum
  • 7. Dysfunction of Frontal Lobe Unilateral Bilateral Either right or left Dominant Both Contralateral hemiplegia Right hemiplegia Broca’s aphasia Bilateral hemiplegia Pseudobulbar palsy Gaze palsy & Head turning Sympathetic apraxia of left hand Gait apraxia Sphincter incontinence Apathy, Loss of initiative Elevation of mood, Increased talkativeness etc. Abulia or Akinetic mutism Rigidity of thinking etc Anosmia Frontal release sign.
  • 8. Dysfunction of Parietal Lobe Either right or left Dominant Nondominant Contralateral hemisensory loss (Hemianaesthesia) Bilateral Ideational apaxia Visuospatial disorder Bilateral Ideomotor apaxia Topographic memory loss Contralateral homonymous inferior quadrantanopia Alexia without agraphia (pure word blindness) Constructional apraxia Dressing apraxia Contralateral Hemineglect Gerstman syndrome • Acalculia • Agraphia • Right left confusion • Finger agnosia Anosognosia Visual inattention Astereognosis/ Tactile agnosia Confusion Agraphesthesia
  • 9. PARIETAL LOBE DYSFUNCTIONS • DOMINANT HEMISPHERE:  Gerstmann’s syndrome  Inferior parietal lobule Tetrad of- Finger agnosia Rt.-Lt.confusion Acalculia Agraphia
  • 10. Dysfunction of Temporal Lobe Unilateral Bilateral Either Rt or left Dominant Nondominant Both Contralateral homonymous superior quadrantanopia Wernicke’s aphasia Inabilty to judge spatial relationship Amnesia (Korsakoff amnesic defect) Seizure Nominal/anomic aphasia Amusia Cortical deafness Deafness Auditory, visual, olfactory and gustatory hallucination Pure word deafness/auditory verbal agnosia Agnosia for sound Apathy Delirium-confusional state Kluver Bucy syndrome Emotional and behavioral change Disturbance of time perception
  • 11. Dysfunction of Occipital Lobe Unilateral Bilateral Either Rt or left Dominant Nondominant Both Contralateral congruent homonymous hemianopia Alexia without agraphia Visual illusion/ Metamorphosia Cortical blindness Anton syndrome Elementary/ unformed hallucination Visual object agnosia Visual halllucination Balint syndrome Hemichromatopsia Loss of topographic memory & visual orientation Prosopragnosia Achromatopsia
  • 12. Clinical Scenario A 60-years-old diabetic & hypertensive male Presented with sudden onset of bilateral visual loss. On examination : Visual acuity - Reduced to hand movement on both eyes. Fundoscopy - Normal on both side. Both direct and consensual light reflex was present bilaterally.
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  • 14. OCCIPITAL LOBE DYSFUNCTIONS BILATERAL OCCIPITAL DISEASE: Cortical blindness
  • 15. OCCIPITAL LOBE DYSFUNCTIONS  Anton’s syndrome  Baliant’s syndrome  Achromatopsia
  • 16. Antons syndrome • Denial of blindness • Patients act as though they could see • Collide with object on attempting to walk • Offer excuse for the difficulties Lesion extends beyond the striate cortex to involve the visual association areas.
  • 17. Clinical Scenario A 50-year-old hypertensive male presented with history of • Difficulty in seeing objects for last 2 weeks • Required assistance for daily activities…
  • 18. On examination: • He had severe difficulty in – pursuit eye movement on both side and – reaching out to objects held by the examiner. • He could recognize a key & a pen individually, but failed to identify them when presented simultaneously .
  • 19. Balint syndrome . A triad of - (1) Optic ataxia (2) Oculomotor apraxia (3) Simultanagnosia. Cause : Stroke involving bilateral parieto-occipital area of brain (border zone between Brodmann area 7 & 19)
  • 21. The Disconnection Syndrome • Interregional connections of the cerebrum are required for all natural sensory and motor functions. • Lesions of the cerebral connecting pathways are known as Disconnection syndrome. • Two types- – Intrahemispheric – Interhemispheric
  • 22. Intrahemispheric Disconnection Syndrome Conduction aphasia – Fluent paraphasic speech – Relatively preserved comprehension – Severely impaired repetition Site of Lesion: Arcuate fasciculus
  • 23. Intra hemispheric Disconnection Syndrome (cont.) • Pure word deafness : Lesion in the left superior temporal gyrus Interruption of connection between the primary & association auditory cortex, also with language network resulting- • Impaired comprehension of spoken words • Impaired repetition • No hearing defect • Nonverbal sound can be heard without difficulty
  • 24. Interhemispheric Disconnection Syndrome Alexia without agraphia • Inability to read • Color anomia & difficulty in copying word may be present. • No difficulty in repetition, writtng or naming objects Site of Lesion: Splenium & dominant occipital lobe
  • 25. Interhemispheric Disconnection Syndrome (cont.) Lesion of the entire corpus callosum • Unable to match an object held in one hand with that in the other • Unable to match objects seen in either half of visual field • Unable to name object held in left hand. • Alexic in left visual field. Congenital agenesis of corpus callosum
  • 26. Interhemispheric Disconnection Syndrome (cont.) Lesion anterior part of Corpus callosum (posterior to genu but anterior to spenium) – Apraxia of the left sided limbs.
  • 28. DISORDERS OF CEREBRUM Vascular diseases: Ischaemia Haemorrhage
  • 29. Case scenario A 77-year- old woman presented with the sudden onset of left-sided weakness and numbness. On examination, in addition to the weakness and sensory loss, she had a left homonymous hemianopia and was unaware of her deficits, denying that there was anything wrong with her. Her eyes were deviated to the right.
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  • 31. Diffusion-weighted sequences Importantly, other diseases, such as active multiple sclerosis (MS) lesions, abscesses, or tumors such as primary CNS lymphoma can also demonstrate restricted diffusion. If there is corresponding hypointensity (referred to as “drop-out”) on the apparent diffusion coeffi cient (ADC) map, then the diagnosis is confirmed in the appropriate clinical setting. .
  • 34. Wake up stroke DWI-FLAIR-mismatch was shown to identify patients within 3–4.5 h with high specificity and positive predicted value PWI-DWI mismatch
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  • 37. Case scenario A 76-year-old man with hypertension and diabetes underwent a coronary bypass artery graft that was complicated by severe blood loss. When he awoke, he was unable to move his proximal right arm and would not speak unless he became upset.
  • 39. Case scenario A 65-year-old man presented with confusion and cortical blindness. His blood pressure in the emergency room (ER) was 231/180.
  • 41. Posterior reversible encephalopathy syndrome PRES PRES Occurs in the setting of rapid,severe increases in blood pressure It presents with a combination of visual loss, seizures,headaches, and altered mental status.
  • 42. CNS Vasculitis • Ischemic stroke is the most common CNS presentation. • However, patients may suffer from a wide range of clinical presentations including hemorrhages, meningitis, and cognitive dysfunction. • Involvement of the extracranial vessels leads to headaches, visual loss, jaw claudication, and cranial tenderness. • Systemic symptoms such as fever, weight loss, and malaise
  • 44. Case scenario • A 30-year-old female presented with double vision and ataxia. Three years earlier she had an episode where she lost vision in her left eye for two weeks. On examination, she was mildly ataxic, with brisk reflexes, and both horizontal and vertical nystagmus.
  • 46. Case scenario • An 18-year-old boy presented with seizures with altered level of consciousness. His attendent also gives the h/o fever, headache , lethargy, myalgia , malaise, fever, and vomiting for 7 days
  • 47. ADEM
  • 48. CASE SCENARIO • A 25-year-old woman had repeated episodes of the sudden onset of fear on unpleasant odor. These were followed by her losing consciousness for several minutes and making bizarre lip-smacking movements.
  • 50. CASE SCENARIO • A 23-year-old female presented with a cluster of seizures. She was otherwise healthy. She had been acting oddly for the past two weeks. She was thinking that her neighbors were spying on her. She was found missing two days prior to her presentation in the emergency room. The patient was diaphoretic on exam and appeared paranoid about hospital staff.
  • 52. CASE SCENARIO • A 30-years-male known case of VSD presented with headaches and left-sided weakness.
  • 54. CASE SCENARIO • A 28-year-old man developed Headache ,vomiting , diplopia O/E There is left sided abducens nerve palsy with bilateral Papilledema
  • 56. Case scenario • A 65-year-old woman presented with personality changes, paranoia, and confusion over the course of several months. On exam, she had mild bilateral papilledema and weakness of her legs.
  • 58. Case scenario • A 56-year-old man presented to the hospital with a seizure. He had been complaining of headaches for the past several months and becoming “slow” as per family. • He also noticed that he was “bumping into things” for the past few months.
  • 60. Case scenario • A 67-year-old man presented with a partial seizure with secondary generalization. • His daughter said that he had been increasingly confused over the past few weeks. • He has significant smoking history
  • 63. Case scenario A 72-year-old woman was brought in by her family. The patient herself said that she felt well, but her family said that she had been “forgetting everything” recently. For example, she would purchase the same products at the grocery store, forgetting that she had bought them only several days earlier. She had also become paranoid, feeling that someone was moving her glasses and wallet. She had no awareness of her deficits.
  • 65.
  • 66. Case scenario • 50 years old male, presented with complaints of forgetfulness, talking irrelevantly since last 18 months. Patient developed symptoms of confusion, ataxia, and altered behaviour 2 years back, for which he was treated as a case of encephalitis. He later progressed to show symptoms of amnesia. Neurological examination revealed MMSE 15/30 ,absent deep tendon reflexes
  • 67.
  • 68. Case scenario • A 65-year-old man presented with rapid-onset dementia. • On exam, he knew his name, but not his age or the location. He thought he was in his office , though he had not worked in several months. He hada profound startle response to any unexpected noise..
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  • 70.
  • 71. Case scenario • A 59-year-old woman presented with several falls. On examination, she had asymmetric rigidity with a shuffling gait. She also developed uncontrolled movements of her left arm.
  • 72. An 8-year-old boy presented with progressive dementia, blindness, and seizures.
  • 73. DISORDERS OF CEREBRUM Inborn error of metabolism: Leukodystrophy Canavan disease
  • 74. Case scenario • An 8-year-old boy presented with mental retardation and seizures since infancy. He had a large “port-wine stain” on his upper face on the right side.
  • 75. Case scenario • An 8-year-old child with MR developed intractable seizures and mental retardation. • The patient had autistic features and language delays, but no focal motor or sensory deficits.
  • 77. DISORDERS OF CEREBRUM Developmental Disorders: Lissencephaly (Agyria) Pachygyria/Polymicrogyria Holoprocencephaly (lobar/alobar) Agenesis of corpus callosum
  • 78. Apraxia A disorder in which an attentive patient loss the ability to execute previously learned activities in the absence of weakness, ataxia, sensory loss or extrapyramidal derangement that would be adequate to explain the deficit – Ideomotor apraxia – Ideational apraxia – Oral buccal lingual apraxia – Gait apraxia – Constructional apraxia – Dressing apraxia
  • 79. Disorders of speech and language
  • 81. Aphasia Anomic aphasia Conduction Transcortical sensory Wernicke Transcortical motor Broca Mixed transcortical Global Aphasia Fluency Comprehension Repetition + - + - + - + - + - + - + -
  • 82. Aphasia Type Fluency Comprehension Repetition Naming Broca’s Impaired Preserved Impaired Impaired Wernicke’s Preserved Impaired Impaired Impaired Global Impaired Impaired Impaired Impaired Transcortical motor Impaired Preserved Preserved Impaired Transcortical sensory Preserved Impaired Preserved Impaired Isolation Impaired Impaired Preserved Impaired Conduction Preserved Relatively Preserved Impaired Impaired Anomic/ nominal Preserved Preserved Preserved Impaired
  • 84. • Known as dementia • Defined by involvement of multiple cognitive domains (memory, intellect, personality, affection &mood) • Causes may be reversible or irreversible • Manifested by several ways • Assessed by MMSE • Treatment according to aetiology • Prognosis variable
  • 85. Dementia Reversible causes Irreversible causes Hypothyriodism Thiamine deficiency Vitamin B12 deficiency Normal pressure hydrocephalus Subdural hematoma Chronic infection Brain tumor Drug intoxication Autoimmune encephalopathy Alzheimer’s Frontotemporal dementia Vascular Parkinson’s Dementia with lewy bodies Huntington’s Leukoencephalopathies