Lec 2 Neuroembyology

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    CENTRAL NERVOUS SYSTEM

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    LEARNING OBJECTIVES

    Formation of notochord, neural plate, and neural

    folds.

    Formation of the neural tube and description of its

    dilatations. Development of spinal cord, differentiation of

    neuroepithelial cells, and formation of spinal

    nerves.

    Congenital malformations including neural tube

    defects of spine (spina bifida).

    Ventricular system development and its

    abnormalities.

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    LEARNING OBJECTIVES

    Development of medulla oblongata, pons, andcerebellum.

    Development of mid brain.

    Structures developing from diencephalon andtelencephalon including development of pituitarygland.

    Cranial nerve nuclei origins in brain.

    Development of peripheral nervous system. Neural crest cells and their derivatives.

    Neural tube defects affecting brain (anencephaly,meningocele, meningoencephalocele,meningohydroencephalocele).

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    Changes in the Germ disc3rdweek

    The ectodermal layer of the disc differentiates into three

    functional zones

    Surface ectoderm

    Neuro ectoderm

    Primitive streak

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    Primitive streak

    Cells in the caudal part of the germ disc proliferate to form a

    linear opacity known as primitive streak

    These are plur ipotent cel ls

    It is considered that the primitive streak gives rise to a new

    wave of cells to all the germ layers

    Therefore forming definitive endoderm & ectoderm

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    NOTOCHORD

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    NEURAL PLATE

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    NEURAL TUBE

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    NEURAL TUBE

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    NEURAL TUBE

    Cranial part gives rise to brain and consistsof:

    3 Dilatations

    Prosencephalon

    Mesencephalon

    Rhombencephalon

    2 Flexures

    Cephalic flexure

    Cervical flexure

    Caudal part gives rise to spinal cord.

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    SPINAL CORD

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    SPINAL CORD

    CENTRAL CANAL

    3 LAYERS

    NEUROEPITHELIAL

    MANTLE

    MARGINAL

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    NEUROEPITHELIAL CELLS

    DIFFERENTIATION OF

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    DIFFERENTIATION OF

    NEUROEPITHELIAL CELLS

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    MANTLE LAYER

    GRAY MATTER OF SPINAL CORD

    BASAL PLATES

    ALAR PLATES

    ROOF PLATES

    FLOOR PLATES

    VENRAL HORN DORSAL HORN

    INTERMEDIATE HORN

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    MANTLE LAYER

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    FORMATION OF NEURON

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    SPINAL NERVES

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    MYELINATION

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    POSITIONAL CHANGES OF THE

    CORD

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    CONGENITAL ABNORMALITIES

    OF SPINAL CORD

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    SPINA BIFIDA

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    BRAIN

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    NEURAL TUBE

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    NEURAL TUBE

    VENTRICLES OF BRAIN

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    VENTRICLES OF BRAIN 4 in number.

    2 lateral ventricles present in telencephalon.

    3rd ventricle in diencephalon.

    4th ventricle in rhombencephalon.

    Lateral ventricles open into 3rd ventricle through

    foramen of Munro. 3rd and 4th ventricles are connected through aqueduct

    of Sylvius present in the mesencephalon.

    4th ventricle opens into subarachnoid space through amedial opening, the foramen of Magendie and 2lateral openings, the foramina of Luschka.

    4th ventricle is continuous with central canal of spinalcord.

    FORMATION OF FLEXURES

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    FORMATION OF FLEXURES

    Cephalic flexure Bt fore

    and hind brain. Present in mid

    brain region.

    Cervical flexure Bt

    medulla and spinal cord.

    Rhombencephalicisthmus Bt Mesencephalon and

    Rhombencephalon

    Pontine flexure Bt

    Mylencephalon andMetencephalon

    Telencephalic flexure Bt

    telencephalon and

    diencephalon.

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    PROSENCEPHALONTELENCEPHALON

    (CEREBRAL CORTEX, CAUDATE AND

    LENTIFORM NUCLEI) AND DIENCEPHALON

    (PINEAL BODY, THALAMUS,

    HYPOTHALAMUS, NEUROHYPOPHYSIS OF

    THE PITUITARY GLAND, MAMILLARY BODY,SUBTHALAMIC NUCLEUS, RETINA).

    MESENCEPHALON (MID BRAIN)

    SUBSTANTIA NIGRA, NUCLEUS RUBER. RHOMBENCEPHALONMETENCEPHALON

    (PONS AND CEREBELLUM) AND

    MYLENCEPHALON (MEDULLA OBLONGATA)

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    MYLENCEPHALON

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    MYLENCEPHALON

    METENCEPHALON

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    METENCEPHALON

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    CEREBELLUM

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    CEREBELLUM

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    PONS

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    MESENCEPHALON (MID BRAIN)

    PROSENCEPHALON

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    PROSENCEPHALON

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    CEREBRAL HEMISPHERE

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    DIENCEPHALON

    PITUITARY GLAND

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    PITUITARY GLAND

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    PITUITARY GLAND

    RATHKES POUCH

    ADENOHYPOPHYSIS, PARS

    TUBERALIS, PARS INTERMEDIA. DIENCEPHALON (INFUNDIBULUM)

    NEUROHYPOPHYSIS (PARS

    NERVOSA), STALK.

    CRANIAL NERVES

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    CRANIAL NERVESTelencephalon Olfactory (I) Sensory

    Diencephalon Optic (II) Sensory

    Mesencephalon Oculomotor (III)

    Trochlear (IV)

    Motor,

    parasympathetic

    Motor

    Metencephalon Trigeminal (V)

    Abducens (VI)Facial (VII)

    Vestibulocochlear

    (VIII)

    Sensory, motor

    MotorSensory, motor,

    parasympathetic

    Sensory

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    CRANIAL NERVES

    Mylencephalon

    Cervical spinalcord

    Glossopharyngeal

    (IX)

    Vagus (X)

    Accessory (XI)

    Hypoglossal (XII)

    Spinal accessorynerve (XI).

    Sensory, motor,

    Parasympathetic

    Sensory, motor,

    Parasympathetic

    Motor

    Motor

    Motor

    SYMPATHETIC NERVOUS

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    SYMPATHETIC NERVOUS

    SYSTEM

    PARASYMPATHETIC NERVOUS

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    PARASYMPATHETIC NERVOUS

    SYSTEM

    NEURAL CREST CELLS

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    NEURAL CREST CELLS

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    Derivatives of neural crest Dorsal nerve root ganglia (sensory) in spinal cord.

    Preaortic ganglia of sympathetic system Parasympathetic ganglia of cranial nerves like ciliary,

    submandibular, sphenopalatine, and otic ganglia.

    Parasympathetic ganglia of GI tract and pelvic viscera

    Schwann cells Adrenal medulla

    Melanoblasts

    Chromaffin tissue

    Parafollicular C cells of thyroid Bones of face and part of vault of skull

    Derivatives of first, second, and third pharyngeal cartilages

    Conotruncal cushions in the cardiovascular system

    Laryngeal cartilages in respiratory system

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    CONGENITAL ABNORMALITIES

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    OSSIFICATION DEFECTS

    MENINGOCELE MENINGOENCEPHALOCELE

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    OSSIFICATION DEFECTS

    MENINGOHYDROENCEPHALOCELE

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    HYDROCEPHALUS

    AQUEDUCTAL STENOSIS

    ARNOLD-CHIARI MALFORMATION

    DANDY-WALKER SYNDROME

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    EXENCEPHALY FAILURE OF

    CLOSURE OF CEPHALIC PART OF

    NEURAL TUBE.

    ANENCEPHALY

    MICROCEPHALY

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    HOLOPROCENCEPHALY Loss of

    midline structures in the brain and face.

    SCHIZENCEPHALY Large clefts in the

    cerebral hemispheres.

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    HYPOPHYSEAL DEFECTS

    PHARYNGEAL HYPOPHYSIS

    CRANIOPHARYNGIOMA

    CONGENITAL MEGACOLON

    (HIRSCHSPRUNG DISEASE) Due to

    defective migration of neural crest cells tothe gut to form its nervous plexus.