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30 Cards in this Set

  • Front
  • Back
Primary vs secondary neurulation
Primary - neuroal tube formation from L1-cranially
Secondary is formation of caudal neural tube from the caudal eminence.
What protein causes neural plate to form
SHH
What do the neural crest cells differentiate into?
1) DRG
2) sensory ganglion for cn 5,7,8,9,10
3) Sympa/para gnaglion
4) chromaffin cells (adrenal medulla)
5) Melanocytes
6) Leptomeninges (pai and arachnoid)
7) Schwann cells
Placdoes
Induced to become neural crest like cells. become:
-olfactory epithelium
-lens of eye
-hair cells of inner ear
-parts of ganglia of cn 5, 7-10
Alar plate
Derived from dorsal thickening of mantel layer. Becomes sensory
Basal Plate
Derived from ventral thickening of mantel layer. Becomes motor.
Sulcus limitans
Seperates the alar and basal plates.
What signaling molecules signal the formation of the basal and alar plates
SHH released by the floor plate leads to basal plate formation
BMP released by roof plate leads to alar plate formation
What do the ventricular, mantel and marginal layers become in the spinal cord
ventricular zone - ependymal layer that lines central canal.
mantle layer - grey matter
marginal layer - white matter
Ventral induction
process by which rostral end of neural tube develops into brain
Retinoic acid
teratagen which modulates hox gene expression altering hindbrain development
Anencephaly
failure of anterior neuropore to close, fatal, not much brain
Encephalocele
Partial failure of the anterior neuropore to seal.
-meningocele
-meningoencephalocele (meninges + brain)
-meningohydroencephalocele - all + ventricular system
Arnold-chiari malformation
vermis herniates through foramen magnum, get hydrocephalus (dialtion of ventricles with csf) and syringomyelai (fluid filled cavity in spinal cord)
Spina bifida
Failure of posterior neuropore to close and failure of vertebral arches to fuse.
spina bifida occulta
least severe, get a hair tuft
meningocele
spina bifida with meninges protruding
meningomyelocele
spina bifida with part of spinal cord protruding
Rachischisis
spinal bifida where spinal cord is esposed to surface, most severe
Hirschsprungs disease
Neurocristopathy. Absesnce of para ganglia in colon. Get megacolon, constipation.
Dandy walker malformation
due to improper formation of the rhombic lip:
-agenisis of cerebellar vermis
-dilation of 4th ventricle
-enlarged posterior fossa
Holoproencephaly
Failure of proencephalon to cleave. Caused by mutation in SHH. Get 1 large brain and associated with shit like cyclopia and cleft palate
Schizencephaly
disorder of neuronal migration, not proper cortex, get developmental delay and siezures.
Lissencephaly
Defect in cell migration of cerebral neurons, dont have gyri
heterotopias
cortical neurons fail to reach cortes, get islands of gray matter.
perinatal hypoxic ischemia encephalopathy
Accounts for 30-70% of neonatal seizures.
Hypoxic hypoxia - diffuse damage to BG, thalamus, hippocampus
Ischemic hypoxia - damage to watershed (boundry zones) which are areas between 2 arterial systems which only recieve the small terminal twigs.
Erbs palsy
C5-C6 lesion, effects from deltoid to brachioradialis. Extension and pronation of the elbow
Klumpkes paralysis
C8-T1 lesion, hand muscles paralyzed. Damage to cervial sypas can lead to horners syndrome - miosis, ptnosis,
Grades of intraventricular hemmorhage
Grade 1 - Originates in periventricular germinal matrix, near head of caudate.
2 - ruptured into lateral ventricle
3 - ventricular dilation due to hemorrhage
4 - extends into brain itself
periventricular leukomalacia
deep white matter has poor perfusion, immature oligos are also prone to damage, leads to brain damage, cerebral palsy, spastic diplegia