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183 Cards in this Set
- Front
- Back
3 axes of limb elongation
|
proximo-distal
antero-posterior dorso-ventral |
|
limb elongation occurs along ___ axis
and is driven by ___ released from ___ and nested expression of ___ |
proximo-distal
FGF apical epidermal ridge (AER) Hoxa genes |
|
antero-posterior differentiation of limb is driven by ___ which originates at ___
|
Shh gradient
zone of polarizing activity (ZPA) |
|
dorso-ventral differentiation of limb is driven by ___ released from ___
|
WNT-7
AER |
|
hCG secretion begins with ___
|
implantation
|
|
peak susceptibility to teratogens is during ___
this corresponds to ___ |
weeks 3--8
organogenesis |
|
genitalia are male/female at week ___
|
10
|
|
rule of 2's
|
2nd week
2 germ layers 2 cavities (amnion, yolk sac) 2 placental components |
|
rule of 3's
|
3rd week
3 germ layers |
|
rule of 4's
|
4th week
4 heart chambers 4 limb buds |
|
2 embryonic layers in thyroid
|
endoderm (follicular cells)
neural crest (parafollicular cells) |
|
2 embryonic layers in adrenals
|
mesoderm (cortex)
neural crest (medulla) |
|
2 embryonic layers in heart
|
mesoderm (myocardium)
neural crest (aorticopulmonary septum) |
|
2 kinds of ectoderm in eye
|
surface ectoderm (lens, epitelial lining of retina)
neuroectoderm (retina) |
|
VACTERL is ___
these are all ___ defects |
vertebral
anal atresia cardiac TE fistula renal limb defects mesoderm |
|
fetal damage from ACEI
|
renal
|
|
fetal damage from alkylating agents
|
missing fingers
|
|
fetal damage from aminoglycosides
|
CN8
|
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fetal damage from cocaine
|
abruptio plancentae
|
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fetal damage from DES
|
vaginal clear cell adenoca
|
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fetal damage from folate antagonists
|
NTD
|
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fetal damage from iodide deficiency
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congenital hypothyroidism
|
|
fetal damage from iodide excess
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congenital goiter
|
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fetal damage from Li
|
atrialized RV (ebstein's anomaly)
|
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fetal damage from maternal DM
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caudal regression
|
|
caudal regressinon may present as ___ (2)
|
anal atresia
sirenomyelia |
|
fetal damage from smoking (4)
|
preterm labor
placental problems IUGR ADHD |
|
fetal damage from tetracyclines
|
discolored teeth
|
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fetal damage from VPA
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NTD (from folate malabsorption)
|
|
fetal damage from vitamin A (2)
|
cleft palate
cardiac defects |
|
fetal damage from warfarin
|
bone deformities
fetal hemorrhage |
|
___ is the leading cause of fetal malformations in the US
|
fetal alcohol syndrome
|
|
fetal alcohol syndrome includes (7)
|
developmental retardation
microcephaly holoprosencephaly facial abnormalities limb dislocation heart fistula lung fistula |
|
mechanism of fetal alcohol syndrome
|
inhibited cell migration
|
|
chorion forms at day ___
amnion forms at day ___ |
3
8 |
|
3 possible chorionicity/amnionicity combinations for twins
|
dichorionic diamniotic
monochorionic diamniotic monochorionic monoamniotic |
|
dichorionic diamniotic pregnancy happens when ___ (2)
|
zygote splits before day 3
dizygotic pregnancy |
|
monochorionic diamniotic pregnancy happens when ___
|
zygote splits between days 3 and 8
|
|
monochorionic monoamniotic pregnancy happens when ___
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zygote splits after day 8
|
|
risk of conjoined twinning occurs with ___ pregnancy
|
monochorionic monoamniotic
|
|
hCG is made by ___
it does ___ during ___ it resembles ___ in structure |
syncitiotrophoblast
makes corpus luteum secrete P 1st trimester LH |
|
maternal side of placenta
|
decidua basalis
|
|
3 layers between fetal vessel and maternal blood/tissue
|
mesoderm
cytotrophoblast syncytiotrophoblast |
|
normal contents of umbilical cord (4)
|
2 umbilical arteries
1 umbilical vein urachus |
|
umbilical abnormality associated with congenital anomalies
|
single umbilical a.
|
|
umbilical arteries and veins are derived from ___
|
allantois
|
|
allantois forms from ___ near ___ which inserts into ___,
which becomes ___ this occurs at ___ week |
yolk sac
hindgut body stalk umbilical cord 3rd |
|
allantois becomes ___
this does ___ |
urachus
conveys urine from bladder to yolk sac |
|
4 urachal abnormalities
|
patent urachus
vesicourachal diverticulum urachal sinus urachal cyst |
|
patent urachus pw
|
urine from umbilicus
|
|
urachal sinus pw
|
recurrent infection
|
|
vitelline duct connects ___ and ___
it is aka ___ it closes at ___ |
midgut
yolk sac omphalomesenteric duct 7th week |
|
4 vitelline duct abnormalities
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vitelline fistula
Meckel's diverticulum vitelline sinus vitelline duct cyst |
|
vitelline fistula pw
|
feces from umbilicus
|
|
Meckel's diverticulum may have ___ mucosa
|
gastric
pancreatic other |
|
Meckel's diverticulum most commonly pw ___ but may have ___
|
painless melena
RUQ pain |
|
Meckel's scan uses ___ to detect ___
|
Tc99
gastric mucosa |
|
truncus arteriosus becomes ___ (2)
|
ascending aorta
pulmonary trunk |
|
bulbus cordis becomes ___ (2)
|
RV
LVOT |
|
primitive ventricle becomes ___
|
LV
|
|
primitive atria become ___ (2)
|
trabeculated RA
trabeculated LA |
|
sinus venosus becomes ___ (3)
|
smooth part of RA
oblique vein of LA coronary sinus |
|
L horn of sinus venosus becomes ___
|
coronary sinus
|
|
R horn of sinus venosus becomes ___
|
smooth part of RA
|
|
SVC is made from ___ (2)
|
R common cardinal vein
R anterior cardinal vein |
|
aorticopulmonary septum develops from ___ to __ and becomes ___
|
superior
inferior membranous IV septum |
|
ostium primum is bounded by ___ from above and ___ from below
septum primum grows from ___ to ___ |
septum primum
posterior endocardial cushion cardiac base posterior endocardial cushion |
|
ostium secundum develops from ___
|
perforations in septum primum
|
|
septum secondum develops at ___
as it grows, ___ regresses it grows until it reaches ___ |
R of ostium primum
top part of septum primum top edge of bottom part of septum primum |
|
4 hematopoietic tissues in fetus, in order of action
|
yolk sac
liver spleen bone marow |
|
yolk sac makes blood from week ___ to ___
|
3
8 |
|
liver makes blood from week ___ to ___
|
6
30 |
|
spleen makes blood from week ___ to ___
|
9
28 |
|
bone marrow makes blood from week ___ to ___
|
28
death |
|
O2 sat in umbilical vein
|
80%
|
|
3 shunts in fetal circulation
|
ductus venosus
foramen ovale ductus arteriosus |
|
ductus venosus takes blood from ___ to ___, bypassing ___
|
umbilical vein
IVC hepatic circulation |
|
formen ovale takes blood from ___ to ___, bypassing ___
|
RA
LA lungs |
|
ductus arteriosus takes blood from ___ to ___, bypassing ___
|
pulmonary trunk
descending aorta lungs |
|
as a rule, blood from ___ goes through foramen ovale, and
blood from ___ goes through RV |
IVC
SVC |
|
after first breath ___ causes ___, causing closure of foramen ovale;
___ causes ___ causing closure of ductus arteriosus |
drop in pulmonary pressure
increased LA P O2 rise PG drop |
|
umbilical vein becomes
|
ligamentum teres hepatis
|
|
umbilical arteries become
|
medial umbilical ligaments
|
|
ductus venosus becomes
|
ligamentum venosum
|
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foramen ovale becomes
|
fossa ovalis
|
|
allantois becomes ___ which becomes ___
|
urachus
median umbilical ligament |
|
embryo has ___ aortic arches
|
6
|
|
1st aortic arch gives rise to ___
|
part of maxillary a.
|
|
2nd aortic arch gives rise to ___ (2)
|
stapedial a.
hyoid a. |
|
3rd aortic arch gives rise to ___ (2)
|
common carotid a.
proximal internal carotid a. |
|
4th aortic arch gives rise to ___ (2)
|
aortic arch (on L)
proximal subclavian (on R) |
|
5th aortic arch gives rise to ___
|
nothing!
|
|
6th aortic arch gives rise to ___ (2)
|
proximal pulmonary a.s
ductus arteriosus |
|
4 conditions associated wtih holoprosencephaly
|
Patau
fetal alcohol syndrome cleft lip cleft palate |
|
dandy walker malformation includes (3)
it is associated with ___ |
absent cerebellar vermis
enlarged 4th ventricle cysts at internal skull base spina bifida |
|
dandy walker malformation pw (4)
|
macrocephaly
cerebellar dysfunction vomiting seizures |
|
3 parts of branchial apparatus
|
arches
clefts pouches |
|
branchial clefts are made from ___
|
ectoderm
|
|
branchial arches are made from ___
|
mesoderm
|
|
branchial pouches are made from ___
|
endoderm
|
|
1st branchial cleft becomes ___
|
external auditory meatus
|
|
2nd-4th branchial clefts become ___
|
cervical sinuses
|
|
persistent cervical sinus becomes ___
|
branchial cleft cyst
|
|
4 cartilaginous derivatives of 1st arch
collectively they are called ___ |
mandible
malleus incus spheno-mandibular ligament Meckel's cartilage |
|
5 muscles derived from 1st arch
|
muscles of mastication
mylohyoid anterior belly of digastric tensor tympani tensor veli palatini |
|
1st arch muscles are innervated by ___
|
V2
V3 |
|
artery derived from 1st arch
|
maxillary
|
|
4 cartilaginous derivatives of 2nd arch
collectively these are called ___ |
stapes
styloid process lesser horn of hyoid stylohyoid ligament Reichert's cartilage |
|
muscles derived from 2nd arch (4)
|
muscles of facial expression
stapedius stylohyoid posterior belly of digastric |
|
2nd arch muscles are innvervated by ___
|
CN7
|
|
2 arteries derived from 2nd arch
|
stapedial
hyoid |
|
cartilaginous derivative of 3rd arch
|
greater horn of hyoid
|
|
muscle derived from 3rd arch
|
stylopharyngeus
|
|
muscle of 3rd arch is innervated by
|
CN9
|
|
2 cartilaginous derivatives of 4th arch
|
thyroid cartilage
epiglottic cartilage |
|
3 muscles derived from 4th arch
|
pharyngeal constrictors
levator veli palatini cricothyroid |
|
4th arch muscles are innervated by ___
|
superior laryngeal branch of CN10
|
|
3 cartilaginous derivatives of 6th arch
|
cricoid
arytenoid corniculate |
|
muscles derived from 6th arch
|
intrinsic muscles of larynx except cricothyroid
|
|
6th arch muscles are innvervated by ___
|
recurrent laryngeal branch of CN10
|
|
treacher collins is caused by problem with ___ arch
it is caused by deficient ___ |
1st
neural crest cell migration |
|
pharyngo-cutaneous fistula is caused by ___
|
persistence of 3rd branchial cleft and pouch
|
|
posterior 1/3 of tongue is formed by arches ___
|
3
4 |
|
1st branchial pouch becomes (3)
|
eustachian tube
middle ear cavity mastoid air cells |
|
2nd branchial pouch becomes
|
epithelium of palatine tonsil
|
|
dorsal wings of 3rd branchial pouch become
|
inferior PT glands
|
|
ventral wings of 3rd branchial pouch become
|
thymus
|
|
4th branchial pouch becomes (2)
|
superior PT glands
parafollicular C cells |
|
5th branchial pouch becomes
|
parafollicular C cells
|
|
DiGeorge is problems with ___
|
3rd + 4th pouches
|
|
3 tumors of MEN 2A
they are all derived from ___ they are caused by ___ |
pheochromocytoma
parathyroid medullary thyroid neural crest cells RET protooncogene mutation |
|
___ is formed by contact of 1st branchial cleft with 1st branchial pouch
this becomes ___ |
branchial membrane
tympanic membrane |
|
anterior 2/3 of tongue is from ___ arch
touch is from ___ taste is from ___ |
1st
V3 CN7 |
|
posterior 1/3 of tongue is from ___ arch
touch is from ___ taste is from ___ |
3rd
CN9 CN9 |
|
extreme posterior of tongue is from ___ arch
touch is from ___ taste is from ___ |
4th
CN10 CN10 |
|
taste fibers from ___ go to ___ nucleus
|
CN7
CN9 CN10 NTS |
|
thyroid originates from ___ which becomes ___
|
pharyngeal endoderm
foramen cecum |
|
during descent of thyroid it is connected to ___ by ___
|
foramen cecum
thyroglossal duct |
|
thyroglossal duct may persist as ___ (2)
|
pyramidal lobe of thyroid
thyroglossal duct cyst |
|
thyroglossal duct cyst may be distinguished from branchial cleft cyst by ___ (2)
|
location
movement on swallowing (thyroglossal will move) |
|
cleft lip is caused by failure of ___ (2) to fuse
these form ___ |
maxillary prominence
medial nasal prominence primary palate (palate anterior to incisive foramen) |
|
cleft palate is caused by failure of ___ (3) to fuse
these form ___ |
lateral palatine processes
median palatine process nasal septum 2' palate |
|
4 contributors to diaphragm
|
septum transversum
pleuroperitoneal folds body wall dorsal esophageal mesentery |
|
septum transversum becomes ___ of diaphragm
|
central tendon
|
|
dorsal esophageal mesentery becomes ___ of disphragm
|
crura
|
|
defective closure of rostral fold causes ___
|
sternal defects
|
|
defective closure of lateral fold(s) causes ___ (2)
|
omphalocele
gastroschisis |
|
defective closure of caudal fold causes ___
|
bladder exstrophy
|
|
jejunal, ___ and ___ atresia is caused by ___
pathology is aka ___ |
ileal
colonic vascular accident apple peel atresia |
|
midgut herniates out through ___ at ___
it returns at ___, after which it ___s |
umbilical ring
6th week 10th week rotates around SMA |
|
most common TE fistula has ___ (2)
|
blind upper esophagus
lower esophagus connected to trachea |
|
TE fistula pw (2)
|
cyanosis
choking/vomiting with feeding |
|
prenatal sign of TE fistula
|
polyhydramnios
|
|
CXR sign of TE fistula
|
air bubble (upper esophageal pouch)
|
|
congenital pyloric stenosis usually presents at ___
it is more common in ___s |
2 wks
1st born males |
|
pancreas is derived from ___gut
|
fore
|
|
two components of embryonic pancreas
|
dorsal bud
ventral bud |
|
ventral pancreatic bud makes ___ (3)
|
head
uncinate process main pancreatic duct (Wirsung) |
|
dorsal pancreatic bud makes ___ (4)
|
body
tail isthmus accessory duct (Santorini) |
|
ventral bud rotates in ___ direction (assuming axial view + radiological convention)
|
CCW
|
|
SMA is ___ with respect to body of pancreas,
and ___ with respect to uncinate |
posterior
anterior |
|
2 abnormalities of pancreatic bud fusion
|
annular pancreas
pancreas divisum |
|
annular pancreas can cause ___
|
duodenal stenosis
|
|
in pancreas divisum, ___ and ___ don't connect
|
wirsung
santorini |
|
3 stages of kidney development
|
pronephros
mesonephros metanephros |
|
pronephros develops at ___
mesonephros is present at ___ metanephros first appears at ___ and develops until ___ |
week 4
1st trimester week 5 week 32-36 |
|
metanephros starts as ___ located at ___
|
ureteric bud
caudal end of mesonephros |
|
mesonephros becomes ___ (4)
|
seminal vesicles
epididymis ejaculatory duct ductus deferens |
|
ureteric bud gives rise to urinary system from ___ to ___, inclusively
it is canalized by ___ |
collecting duct
ureter week 10 |
|
___ aka ___ gives rise to urinary system from glomerulus to distal tubule
it is induced by ___ |
metanephric mesenchyme
metanephrogenic blastema ureteric bud |
|
3 effects of oligohydramnios (as in potter's syndrome)
|
limb deformity
facial deformity pulmonary hypoplasia |
|
T/F: horseshoe kidneys function normally
|
true
|
|
horseshoe kidneys fuse at ___
they are trapped by ___ which causes ___ |
inferior pole
IMA they stay low in abdomen |
|
paramesonephric ducts aka ___ become ___ (3)
|
Müllerian ducts
fallopian tubes uterus upper 1/3 of vagina |
|
in men, mesonephric ducts persist because of ___ released by ___
paramesonephric duct development is inhibited by ___ released by ___ |
testosterone
Leydig MIS Sertoli cells |
|
___ drives male genital differentiation
___ drives female |
DHT
E |
|
genital tubercle becomes ___ (3) in men and ___ (2) in women
|
glans penis
corpora cavernosa corpus spongiosum glans clitoris vestibular bulbs |
|
urogenital sinus becomes ___ (2) in men and ___ (2) in women
|
bulbourethral glands (Cowper)
prostate greater vestibular glands (Bartholin) urethral/paraurethral glands (Skene) |
|
urogenital folds become ___ in men and ___ in women
|
ventral shaft of penis
labia minora |
|
labioscrotal swelling becomes ___ in men and ___ in women
|
scrotum
labia majora |
|
hypospadias is caused by ___
epispadias is caused by ___ ___ is more common |
deficient closure of urethral folds
mispositioning of genital tubercle hypospadias |
|
complication of hypospadias
|
UTI
|
|
epispadias is associated with ___
|
bladder exstrophy
|