Embryology Flashcards
(20 cards)
notochord
forms on the midline of the trilaminar embryo from mesoderm
induces overlying ectoderm to thicken and grow into neural plate
becomes future nucleus pulposus
neurulation
16-18 days neural plate formed
19-20 days neural folds elevate, beginning at first 5 somites
21-24 days neural folds begin to fuse, leaving neuropores where neural tube communicates with amniotic sac
25 days - cranial neuropore closes
27 days - caudal neuropore closes
segmentation of neural tube
prosencephalon (becomes diencephalon and telencephalon)
mesencephalon
rhombencephalon (becomes metencephalon and myelencephalon)
myelon
prosencephalon
diencephalon - thalamus, hypothalamus
telencephalon - cerebral hemispheres
mesencephalon
midbrain
rhombencephalon
myelencephalon - medulla
metencephalon - pons, cerebellum
myelon
spinal cord
anencephaly
failure of cranial / anterior neuropore closure
failure to develop brain in cranial vault
spina bifida
failure to close caudal neuropore
occulta - benign, asymptomatic
meningocele - protrusion of meninges
myelomeningocele - protrusion of spinal cord and meninges
rachischisis - open neural tube due to no neural tube elevation
brain volume growth
sulci and gyri form mostly between 20-30 weeks
brain grows mostly from myelination that beings in third trimester and continues after birth
CSF formation
CSF formed in week 5
eyes
begin as ‘optic grooves’ - diverticulae of diencephalon around 24 days
grooves become pouches (vesicles) by day 27
vesicle and stalk invaginate to form the choroid fissure (future iris)
choroid fissure fuses at week 7
neural retina forms from inner layer of optic cup
coloboma (incomplete iris) due to incomplete choroid fissue closure
layers of neural tube (inner to outer)
ventricular - gives rise to neuroblasts
mantle - derived from neuroblasts; becomes gray matter
marginal - fibers of neuroblasts; becomes white matter
spinal cord plates
sulcus limitans divides gray matter into the alar (dorsal) and basal (ventral) plates
DiGeorge Syndrome
deletion on chromosome 22 that causes a neurocristopathy - defect in development of tissues containing cells derived from neural crest
thymic hypoplasia, cleft palate, kidney abnormalities, heart defects, facial abnormalities, no parathyroid
tissues derived from neural crest
pigment, teeth, bones and cartilage of face / neck, parts of glands, adrenal medulla, dorsal root afferent neurons, cranial nerve afferents, schwann cells, parts of the heart
PNS development
neural crest (ectodermal) cells migrate from neural fold through somites to form dorsal root ganglia, sympathetic and parasympathetic postganglionics, cranial nerve sensory ganglia
sympathetic innervation of heart
T1-4
nerves derived from neural crest
afferent dorsal root ganglia
CN sensory
ANS postganglionic
nerves derived from CNS
CN efferent ventral root
CN motor