Embryology Flashcards
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