This document summarizes the anatomy and functions of different areas of the cerebral cortex. It describes the allocortex which makes up 10% of the cortex, and the neocortex which is the remaining 90%. It then discusses the six layers of the neocortex and different cell types. It provides details on agranular and granular cortices and their characteristics. Specific areas of the cortex are then described in more detail such as the frontal, parietal, and polar cortices. The document outlines different classification schemes for cortical areas and focuses on the 52 areas described by Brodmann. It provides in-depth descriptions of the primary motor, premotor, frontal eye field, supplementary motor, and prefrontal cortical areas.
Students are required to know the detailed anatomy of the cortex and also the lesions and their presentation in patients.Medicine in itself derived from a thorough understanding of the anatomy in the initial years of MBBS.Thus it is an iminantory part of this slideshare.
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.
Students are required to know the detailed anatomy of the cortex and also the lesions and their presentation in patients.Medicine in itself derived from a thorough understanding of the anatomy in the initial years of MBBS.Thus it is an iminantory part of this slideshare.
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.
I. Cerebrum
II. Brain Stem
III. Cerebellum.
The Cerebral Cortex
A. Frontal lobe
1) Motor area (area 4):
Frontal lobe
parietal lobe
temporal lobe
occipital lobe
I. Cerebrum
II. Brain Stem
III. Cerebellum.
The Cerebral Cortex
A. Frontal lobe
1) Motor area (area 4):
Frontal lobe
parietal lobe
temporal lobe
occipital lobe
cerebral cortex
cerebral cortex function
cerebrum
functional areas of cerebral cortex ppt
cerebral cortex function psychology
cerebrum function
association areas of the cerebral cortex
anatomy and physiology of temporal lobechaurasia028
this ppt talks about the detailed physiology of temporal lobe and explain in detail about the mechanism involved in speech, auditory response and episodic memory.
it also talks about the anatomy and functions of the temporal lobe.
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
Title: Sense of Taste
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 structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
4. Allocortex – 10 % (also called Limbic Cortex)
i. Archipallium – hippocampus & Dentate gyrus.
ii. Paleopallium – Uncus & part of Parahippocampal
gyrus.
iii. Mesocortex. – transitional zone.
Neocortex (Isocortex) -Rest of 90% of cerebral cortex.
5. Six layers
1. Molecular
2. Outer granular
3. Outer pyramidal
4. Inner granular
5. Inner pyramidal
6. Pleomorphic
Cells:
1. Pyramidal cells of betz
2. Granule (stelate) cells
3. Cells of martinoti
4. Horizontal cells of cajal
6. AGRANULAR CORTEX
Pyramidal cells – large,
Betz cells
Granule cells absent or
less in number
Seen in Motor cortex (4)
& Boca's motor speech
area (44)
GRANULAR CORTEX
Excess granule cells
Few pyramidal cells
Seen in sensory cortex &
visual area, auditory area
7. FRONTAL CORTEX
Small and medium
pyramidal cells
Few stellate cells
Pre-frontal cortex of
frontal lobe
PARIETAL CORTEX
More stellate cells
Seen in most of parietal lobe &
junction of parietal, temporal &
occipital lobes
POLAR CORTEX
Thinnest of all
All layers reduced depth.
Seen in frontal & occipital pole
8. For functional analysis, cerebral
cortex is divided into number
areas,
20 areas of Campbell
109 areas of Economo
200 areas of Vogt
52 areas of brodmann- frequently
used
Subdivided into motor, sensory
and association areas
9.
10.
11. Subdivided into
Primary motor area (area 4)
Pre-motor area (area 6)
Frontal eye field (area 8)
Supplementary motor area
Pre-frontal area (areas 9 to 12)
12. Location:
Precentral gyrus (area 4)
Extends to the ant. part of
paracentral lobule
Agranular cortex
Afferents :
Premotor area (Area 6)
Somesthetic or
somatosensory cortex
Ant. Part ventral nucleus of
thalamus(which receives
info. from cerebellum
Basal ganglia
13. Efferents :
Fibres from area 4 and
area 6 forming…
1. Corticospinal
2. Corticonuclear
3. Corticobulbar tracts.
Regulate the voluntary
movements of opposite
side of body
Fronto-pontine fibres
Corpus striatum, red
nucleus
14. Control movements of
voluntary muscles of opposite
side
Movements represented with
head end below and leg end up
(INVERTED MOTOR
HOMUNCULUS)
Centres from below are: lips,
tongue, larynx, pharynx, face,
head & neck, upper limb with
large area for fingers and hand,
trunk, lower limb above knee.
Ant. Part of paracentral lobule
Extent of area depend on skill of
movement and not on the bulk
of muscle
15. Somewhat sensory. Receive some sensations like
tingling and numbness
Known as MSI
Muscles of forehead, tongue, mastication, larynx,
pharynx, extra ocular bilaterally represented
Only movements not muscles
LESION: initially flaccid paralysis
16. Location (area 6):
In front of area 4, include
post. Part of sup., middle
and inf. Frontal gyri
On medial side, continue
with supplementary motor
area
Agranular & motor
17. Integrates voluntary movements to perform skilful act.
Writing centre
Concerned with programming which is executed by
area 4
LESION:
Produce difficulty in the performance of skilled
movements.
Apraxia: loss of the ability to do simple or routine acts
in the absence of paralysis.
Agraphia: when writing is also involved.
19. Lie in front of area 6
Involve posterior part of middle
frontal gyrus
Agranular cortex
Regulate voluntary conjugate
movements of eye. Deviation of
eyes to the opposite side
Controls voluntary scanning
movements of the eyes and is
independent of the visual
stimuli.
Connected to the visual area of
occipital cortex by association
fibres.
Lesion of the area cause two eye
to deviate to the side of lesion
20. Located on medial surface
of cerebrum in the post.
part of medial frontal gyrus
anterior to the paracentral
lobule
Afferents from VA and VL of
thalamus
Efferents to area 4
Function is to control
complex movements.
Produce sensation of “URGE
TO MOVE’
Receive some senses (MSII)
Lesion of area produce
AKINESIA
21. Rest of frontal lobe ant. to pre-motor
area which include orbital surface also
Fibres from thalamus, hypothalamus,
limbic system, all areas of cortex
Concerned with individual’s
personality
Regulate depth of feeling, thinking,
mature judgement, orientation,
concentration, pleasure and
displeasure, right or wrong.
Bilateral damage due to trauma or
tumour: change in personality, loss of
concentration, judgement,
inappropriate social behaviour like
vulgarity of speech, improper clothing
23. Primary somesthetic
areas (areas 3,1,2)
Secondary somesthetic
area
Somesthetic association
are (areas 5,7)
24. Located in the post-central
gyrus and extends into the
posterior part of the
paracentral lobule on the
medial surface.
Granular cortex
Afferents from VPL and
VPM of thalamus and other
areas of cortex
25. Localise, analyse, discriminate
all modalities of sensations
Sensations represented with
head end below (INVERTED
SENSORY HOMUNCULUS)
Paracentral lobule receive
sense of distension from
bladder and rectum
Hand, face, tongue, lips having
larger representation in cortex
Lower part act as taste centre
(area 43)
Modulate sensory input
Secondarily motor (SMI)
26. Located on the posterior part of posterior ramus of
lateral sulcus
Involve lower part of pre and post-central gyri
Receive mainly pain sensation
Somewhat motor in function (SMII)
27. Located in the superior
parietal lobule
Connected with higher
association area in supra-
marginal gyrus (area 40)
Concerned with the
perception of shape, size,
roughness, and texture of
the objects
Stereognosis- ability to
identify known objects in
hand with closed eyes
Astereognosis or Tactile
agnosia
28. Primary visual area
(area 17)
Visual association
area (area 18 & 19)
Higher visual
association area
(area 39)
29. Located in the lips and walls
of posterior part of calcarine
sulcus which include cuneus
and lingual gyrus
Thinner and granular cortex
Stria of gennari
Afferents from optic radiation
Temporal half of same retina
and nasal half of opposite
retina
Register opposite field of
vision
30. Macular area-
occupying approximately
posterior one-third of the
visual cortex.
is the central area of retina
and responsible for maximum
visual acuity (keenest vision)
has extensive cortical
representation
Connected to area 18, 19 of
both sides
Concerned with reception and
perception of simple visual
impressions like colour, size,
form, transparency etc.
31. Unilateral lesion due to
thrombosis, trauma
produce partial blindness
(hemianopia) with
macular vision retained
Macular sparing because
it is supplied by both
MCA and PCA
32. Occupy rest of occipital
lobe and calcarine sulcus
Afferents from area 17
Occipital eye field-
produce involuntary
deviation of eyes reflexly
33. Located in the angular gyrus
of inferior parietal lobule
It relate visual information
to the past experience, thus
enabling person to
recognize and identify the
object by vision
Lesion of this area- visual
agnosia- inability to
recognize known objects by
vision
Sensory aphasia (word
blindness)- inability to
recognize written word
34. Primary auditory
area (area 41)
Auditory association
area (area 42)
Higher auditory
association area
(Wernicke's area)
(area 22)
35. Involve anterior transverse
temporal gyrus (of
Heschl), on the upper part
of sup. temporal gyrus
Granular cortex
Afferents from MGB as
auditory radiation
Detect the changes in
frequency and direction
from where sound
originates
Unilateral lesion no
deafness due to bilateral
presentation
36. Lie behind area 41
Involve posterior
transverse temporal
gyrus of superior
temporal gyrus
Granular cortex
Same function
37. Wernicke’s area
Rest of the area
Afferents from area 41 &
42
Interpretation of sounds
and comprehension of
spoken language from
past auditory experiences
Lesion produce sensory
aphasia (word deafness)-
unable to interpret the
spoken words.
38. Taste area (area 43)-
lower part of inf. parietal
lobule
Vestibular area- lower
part post-central gyrus
near face area
Olfactory area (area 28)-
anterior part of
parahippocampus gyrus
and uncus
39. Speech- highly complex function
Speech function performed by dominant hemisphere
In 90%, left one, DOMINANT (TALKING BRAIN) &
right one, NON DOMINANT (MUTE BRAIN)
FOUR SPEECH CENTRES: 3 sensory & 1 motor
Sensory speech areas:
1. Area 22 (Wernicke's area)
2. Area 39
3. Area 40
Broca’s motor speech area (area 44 & 45)
40. Area 22 (Wernicke’s area)
Interpret spoken language &
recognize familiar words
Congenital deaf child-
dumb
Area 39 of angular gyrus-
store visual images and
recognize them by sight
Area 40 of supramarginal
gyrus- recognize familiar
objects by touch and
proprioception
All these 3 areas receive
input from hearing,
vision, touch and process
it in the area 22 &
Then project it to Broca’s
area through ARCUATE
FASCICULUS
41. Located in the pars
triangularis and pars
posterior of inferior
frontal gyrus
Afferents from area 22
Efferents to the muscles
of tongue, lips, larynx,
pharynx, palate, face for
production of speech
42. Area 22- word deafness- unable to interpret spoken
words. Speak fluently with incorrect and useless words
Area 39- word blindness- inability to recognize
written words even written by self
Alexia, Agraphia
Area 40- Astereognosis
Area 44 & 45- motor aphasia- cannot speak properly
although he understand everything. Slow speech with
many grammatical mistakes
Conduction aphasia- arcuate fasciculus damage