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01.anatomy Sample
01.anatomy Sample
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GAMETOGENESIS
Oogenesis 00:12:43
month)
filter pubertg :
Ovulation s
e^raV^ian follicle release secondarg oocgte which is in
metaphase arrest.
GcraWtan follicle aVter the release Vorms corpus luteum.
Spermatogenesis 00:31:24
Spermatogenesis Oogenesis
meiosis starts only after meiosis starts by
puberty intrauterine life
Polar bodies are not formed Polar bodies are formed
lprimary spermatocyte will Iprimary oocyte will form
form 4 spermatids Iovum (remaining are
polar bodies)
1 WEEK DEVELOPMENT
ST
Fertilization 00:00:20
Acrosomal
—
Binding to ZP » Acrosomal reaction -4 Release o?
enzymes.
Substances released :
• Acrosin.
• Acid phosphatase.
• Hyaluronidase.
Acrosomal reaction —> Penetration into ZP.
— —
Penetration > Cortical reaction » Cortical enzymes
—
release secretions (cortical granules) > Keach ZP » ZP
changes its permeability -4 Presents polyspermia
—
3. Fusion o? male and female pronucleus.
—
—— —
Zygote » Cleavage > a cell division (a4 hours post
—
Vertilizatior) > 4-cell stage > 8-cell stage > ifo-cell—
stage (morula) » 3a cell stage (advanced morula) >
— —
—
Enters uterine cavity » Cavitation > Blastocyst.
space
• upto 8-cell stage • Totipotent cells +■ cells are loosely
arranged.
Active
AVter 8 cell stage : Compaction (cells attached with
tight junctions).
Hypoblast cells :
• These are cuboidal cells.
Are formed on the ventral aspect of the embryo.
It yives rise to exo coelomic membrane (lined by flat/
squamous cells).
This encloses a cavity called yolh sac.
Extraembryonic mesoderm
Extraembryonic
somatic Amnionic
mesoderm cavrty
- VolK Sac
cavity
splanchnic
mesoderm
Cytotrophoblast coelom
Syncytiotrophoblast
It is synthesized by syncytiotrophoblast.
It stimulates the production 0? proyesterone which is
essential to maintain the preynancy.
HCGj hormone assay is done in :
• The maternal blood : by 8th day.
Motochordal canal
Motochordal plate
De^nrtive notochord
Gastrulation 00:06:19
l. Paraxial mesoderm ;
Forms somites.
A. Intermediate mesoderm :
Forms uroyenital system : Kidney testis, ovary
mesonephric duct, Para mesonephric duct.
5. Lateral mesoderm ;
Cavity in lateral mesoderm Vorms the body cavity (Pleural,
Pericardial, Peritoneal cavity).
i
*
Meural tube
Dermatome (ectoderm)
Somite - muotome
epidermis
(ectoderm)
Sidney and gonads
(intermediate ^ut lining
mesoderm) (endoderm)
Somatic
Splanchnic mesoderm mesoderm
•Visceral serosa • Limb bud
•Smooth muscle o? gut • Parietal
serosa
Peritoneal cavity • Dermis
(coelom)
Divided into 3
• ventral sclerotome ; Body o? vertebra
• Dorsal sclerotome : Spine o? vertebra.
• Lateral sclerotome : Vertebral arch.
Dermomyotome :
Subdivided into dermatome and myotome.
• myotome J Skeletal muscles o? the body.
• Dermatome : Dermal layer o? sKin.
Placenta 00:43:17
Chor ion »
Formed by
• extra embryonic mesoderm.
• Cytotrophoblast.
• Syncytiotrophoblast.
Chorionic Villi $
Firmer lihe projections arising Vrom chorion. 3 types :
• Primary chorionic Villi s
Formed by Cytotrophoblast Syncytiotrophoblast.
Vol* sac
uterine cavity
Placenta
Fused decidua
parietalis, chorion
laeve and amnion
Amniotic caVtty
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Neurulation 00:00:25
space
Active
• migratory cells.
Also called as mesenchymal cells.
Meural tube formation initially occurs at cervical region.
Meural tube communicates with amniotic cavity through •
neuropore :
I. Cranial
Cranial neuropore
• Closes by as*1day.
• Failure to close :
Onencephaly.
• Remnant oV cranial
neuropore : Lamina
terminalis (situated
in the anterior wall
o? 3rd ventricle).
a. Caudal neuropore :
• Closes by aB*1day.
• Remnant is terminal
ventricle.
• Failure to close s Spina
bi^da anomalies.
Caudal neuropore
Anencephaly
rrwMsnoecraior
(m**rarO
<HTX**C^)
Derivatives oV vesicles :
I. Telencephalon : Cerebrum and corpus striatum.
a. Diencephalon :
• Thalamus, hypothalamus, metathalamus,
subthalamus and epithalamus.
• Pars nervosa (posterior lobe o? pituitary).
• Retina and optic nerve.
3. mesencephalon ; midbrain.
4. Rhombencephalon •
• metencephalon : Pons and cerebellum.
• myelencephalon * medulla oblanyata
Ventricles 00:18:40
Active space
Q3 CSF and
Ventricle; Leave Feedbai
Circulation o? CSF 5
Formed in lateral ventricle Foramen o? monro -* 3rd
-*
Applications 00:06:18
Arachnoid VilVi/yranulations :
Site o? absorption o? CSF. Also acts as a valve and prevent
the entry o? venous blood
CSF pressure > venous pressure -* Drains into dural venous
sinus via superior say ittal sinus.
• Acts as a valve and prevents entry o¥ venous blood
Pterion 00:14:14
Dandy-LOalher syndrome :
• Cyst in posterior cranial Vossa.
• Atresia o? Voramen magendi
and Voramen LuschKa.
• 4^ ventricle dilated
Dandy-WalKer syndrome
Posterior horn of
lateral ventricle
Inter ventricular
aqueduct
foramen
ventricle
Thrd ventricle
Infer or horn of
median
lateral ventricle
aperture
Central
Posterior horn of
€>enu of the
the lateral ventre Ie
callosum
Rostrum of
the corpus Stria
callosum terminal is
head of the
caudate rucleus Infer or horn
of the lateral
caudate ventrole
nucleus Anter or
Tail of the
Septal area perforated caudate rucleus
substance nuclei
Occipital horn o¥
right lateral
ventricle
Fibres o?
Optic radiation
?orceps major
medial Lateral
Bulb o?
posterior horn Cavity o?
Calcar avis s
Calcarine sulcus
-
delations o¥ thalamus sagittal section o? brain
body o? ¥orn<x
1. Teymentum of midbrain.
Poor of 3rd ventricle also forms interpeduncular fossa
•
1
Inferior colliculus 1
/ . 5
\ median sulcus 1
f Sulcus lirrwtans i
i •1 R
middle r
/I tl \ / Inferior J peduncles
\\ fj 1 1
I vagal trgone 1
\ 1If/,
\ \ I III '
Cuneate tubercle
Obex
1
\\ / /1 Gracile tubercle
1— Fasciculus cuneatus
1
Fasciculus gracilis 1
median &ulcus 1
medial ernmence
^CuS ittans
k1
1
/ \ Facia) coll iculus
7 vestibulai area
Hypogloss
ingle
2
&
?
1
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SPINAL CORD
Anterior median
Assure
Anterolateral
sulcus
meninges :
It consists o? piamater, arachnoid membrane and dura.
Filum terminate : modification o? piameter from u to coccyx.
Arachnoid membrane ends at lower border of sa. space
Subarachnoid space also ends at lower border of Sa. Active
Plum terminate Cao cm) has a parts :
• Filum terminate internum ( iScm ) : From u to Sa
Present inside the arachnoid membrane.
Dura
mater
Thoracic
spinal nerves
Lumbar
enlaraet
Conus medulians
Lumbar
Cauda equina spinal nerves
Filum
Conus medullaris :
• It is the lower taper ing end o? the spinal cord.
• Sacral and coccygeal nerves are arising Vrom it, only these
nerves are aWected in conus medullar is syndrome.
Cauda equina
• Bunch o? spinal nerves Vrom La to coccyx.
• Lumbar, sacral and coccygeal nerves are involved in
cauda equina syndrome.
Total number o?
• Spinal nerves 31 pairs.
• vertebra 33
Spinal segments do not always correspond with vertebra.
Substatia
Posterior horn (sensory)
e«elat inosa
(Continues as spina) UJhite matter
nucleus o?
Lateral horn (only ?etu)
White matter e<rey matter : collection
collection o¥ axons o¥ cell bodes
Mucleus proprius interior horn (motor)
media) 5 lateral
Mucleus Lateral nucleus
Intermediate nucleus
Clanse's column Visceral afferent media) nucleus
nucleus
Dorsal
column
Fasciculus
gracilis
Fasciculus
cuneatus-
—
Dorsal Lateral corticospinal
—
spinocerebellar tract tract
ventral Rubrospinal tract
spinocerebellar tract • Lateral reticulospinal
Spinotectal tract . tract
Spino-olivary tract vestibulospinal tract
ventral reticulospinal
tract
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Almost all the cranial nerves have bilateral innervation Vrom the
cortex except Vacial nerve. The lower part o? the facial
nucleus is innervated only by the opposite cortex.
opposite side in the spinal cord and then reach the anterior
horn.
upto the anter ior horn, fibres are called as upper motor
Meuron (umM).
The anterior horn and the spinal nerves arising ?rom that are
called as Lower motor neurons (Lmn).
=
Decussation is 100% TS% cross at medullaj cross at spinal
cord
Lesion in the corticospinal tract :
• In the brainstem (above the pyramidal decussation) :
Contralateral weakness.
• In the spinal cord (no fibres come out o? the aV^ected
segment) : Ipsilateral weakness.
• In the midbrain - uieber syndrome $
mid brain
(section at superior colliculus)
Tabes dorsalis
TB spinal segment
impaired proprioception,
space
ihe touch, vibratory sense
and two point
dcscr miration (ipsilateral)
Active
Impaired pain, crude touch and
temperature sensation (Contralateral)
BRAIN STEM
medulla :
medial elevation called pyramid Pyramidal tract.
Lower end o? medulla -* Decussation o? pyramid
Lateral to pyramid -* Olive.
Inside olive -* Inferior olivary nucleus.
Between pyramid and olive XII (Hypoglossal nerve)
ftbers.
Lateral to olive -* IX, X, and XI nerves.
Pons »
Bridge between midbrain and medulla space
a rootlets : Active
l. Large sensory root o? trigeminal nerve.
a. Small motor root o? trigeminal nerve.
Cerebral peduncle :
• Substantia nigra (SM) divides cerebral peduncle into
three parts.
• Tegmentum (area behind Ski).
• Crux cerebri (area in Vront o¥ SM).
space
Active
I. uleber syndrome :
• Lesion -* III nerve + corticospinal tract.
• Features -» i/l LmM III nerve palsy * c/l hemiplegia.
• Crossed hemiplegia.
5. Claude syndrome =
• nerve + red nucleus.
Lesion -* III
• Features -* i/l LmM III nerve palsy + c/l ataxia.
3. Benedict syndrome »
• LOeber + Claude + subthalamus involvement.
• Lesion -* III nerve + corticospinal tract + red nucleus +
subthalamus.
• Features -* i/l LmM ill nerve palsy c/l hemiplegia +
c/l ataxia hemiball ismus.
4. Dorsal midbrain syndrome = Parinaud syndrome :
Mot due to a vascular lesion.
mostly due to tumors/mass.
Ill nerve not involved (as lesion is dorsal).
Mo uoeahness (no corticospinal tract).
• Lesion -* Pretectal nucleus.
• Features upgaze palsy, Argyll Robertson pupil (as
pretectal nucleus is involved in light re^x).
Pons syndromes 00:48:25
l. millard-€\ubler syndrome :
• Features -* i/l LmM Facial nerve palsy + i/l vi nerve
palsy + c/l hemiplegia (due to involvement 0? VI* VII* |
nerve nucleus CST). |
a. Raymond’s syndrome »
• Features -* |/l abducent nerve palsy + c/l hemiplegia
(due to involvement 0? VI* nerve nucleus CST).
Explanation •
Right sided weabness -* Le?t corticospinal tract affected.
LeVt eye down and out, dilated -* CM III a^ected.
Ipsilateral CM 111 palsy + Contralateral Hemiplegia -* LLeber’s.
Q. unable toperform leVt hand ^nger-to-nose test.
Loss o? pain and temperature o? Ie?t Vace.
LeVt eyelid droop j Small pupil.
Loss o¥ pain and temperature o? right arm and leg.
Hoarse voice.
Loss o? gag re$ex o? Ie¥t side o? throat.
Palate raised on right side.
Answer : LeVt lateral medullary syndrome.
Anatomy •v4.0 •Marrow 6.0 •2022
11 7Q
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CEREBELLUM
I. Archeocerebellum/vestibulocerebellum :
* Floculus.
• Module.
• Lingula.
Regulates balance and equilibrium.
Lesion • Loss of balance, ataxia, nystagmus.
a. Paleocerebellum/spinocerebellum :
• Anterior lobe (Al).
• uvula.
• Pyramid.
Regulates tone of the muscles, coordination of movements.
Lesion : Hypotonia.
3.Meocerebellum/cerebrocerebellum ;
Regulates the smooth performance and planning of voluntary space
motor activity. Active
Lesion ’• Dysarthria, dysmetria, dysdiadochohinesia,
intentional tremors.
• Climbing ftber s
Comes Vrom inferior olivorg nucleus o? -the opposite side
(olive in medulla).
It goes to onlg one Purhinje cell.
• mossg Srber :
Divides into 4-S terminals.
Each -terminal Sorms cerebello-glomerulus north granular
cell and golgi cells (Sound in inner granular lager).
T shaped Stber Srom granule cells anastomose with a
large number oS Purhinje cells.
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Complete sulcus :
ore very deep and yive impresston to the lateral
ventricle.
• example : Anterior part o? calcarine sulcus, collateral
sulcus.
• Anterior part o? calcarine sulcus yives impression (calcar
avis) on the medial side o? posterior horn.
• Collateral sulcus yives collateral eminence.
Lesion in the right side frontal eye field : Not able to deviate
the eye to the left side.
byes deviate to the side of the lesion (righO.
Anatomical pathway for horizontal
eye movements
Cingulate gyrus •
• It is a part o? the limbic system.
• Connects sensory inputs to emotions.
• Emotional response to pain.
• Regulation o? aggressive behaviour.
• maternal bonding.
• Decision maKing.
Damage to cingulate gyrus »
• Patients struggle to associate certain actions with
emotions.
• Patients do not realize that their actions can hurt others.
medial
Homunculus
Aphasia '•
• Disorder of language.
• Involves only dominant lobe.
• Comprehension : Stood understanding of written and
spohen language.
Broca’s area :
• motor area for speech.
• In the inferior frontal gyrus.
• Area 44, 45.
LOemiche’s area ;
In the posterior part of superior temporal gyrus.
Area aa.
Receives word as a symbol
To recognise the symbols, fibres are sent to the angular
gyrus.
After recognition, fibers are sent bach to uOemicKe’s
area
uJemiche’s and Broca’s area are connected by means
Is
of arcuate fasciculus.
• Fibres reach broca’s area Anally.
For reprtition of words : Areas aa, 44, 4S should be normal and
connected to each other.
Introduction 00:00:22
3 categories
I. Association f bers : Connect areas within same
hemisphere.
a. Commissural ftbers Interconnect similar regions in both
hemispheres.
3. -
Projection f bers Connect cortical to subcortical
structures
Association fibres 00:02:09
space
Active
Cingulum
Inferior longitudinal fasciculus
Uncinate fasciculus
Applied anatomy :
I. Agenesis o? corpus callosum :
• =
AICAE.OI syndrome X linked dominant disorder,
a. Spirt brain syndrome *
• The two cerebrums are not connected
• Corpus callosum is absent.
examples :
Internal capsule.
Corona radiata.
Fornix (contains all types o? white matter).
Internal capsule :
• Projection Viber.
• Internal capsule is present between caudate nucleus and
thalamus medially.
• LentiVorm nucleus on lateral side.
Parts o? internal capsule =
I. Anterior limb (present between caudate nucleus medially
and lentiVorm nucleus laterally).
a. e^enu (present between anterior limb and poster ior limb).
3. Poster ior limb (present between thalamus medially and
lentiVorm nucleus laterally).
4. £etro lentiVorm part (retro Behind). =
S. Sub-lentiVorm part (sub • Below).
motor Sensory
Anter ior limb Fronto-pontme Anterior thalamic
radiations
Superior
(Dorsal)
ICA
Inferior
(ventral)
BASAL GANGLIA