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22 Cards in this Set

  • Front
  • Back
Notochord develops into...
nucleus pulposus of disc
Craniopharyngioma
bening tumor of Rathke's pouch with cholesterol crystals and calcifications,

adenohypohpyis of pituitary
Agensis vs. aplasia
aplasia- absent organ despite primordial tissue being present

agenesis- no primodial tissue
Fetus most suceptible in 3-8th weeks to teratogens... what happens with lithium, valporate and phenytoin
lithium- atrialized RV

valproate- neural tube defects

phenytoin- fetal hydantoin syndrome, microcephaly, weird facial features, hypoplastic nails, distal phalanges, ardiac defects, MR, small
Meckel's diverticulum
partial closure with paten portion attached to ileum, possible ectopic gastric mucosea, melena and periumbilical pain. Child with noninfectious bloody stool, 2 feet from ileocecal valve
Formation of interventricular septum
1. muscular ventricular septum forms, leaving an opening
2. AP septum meets and fuses with muscular to form membranous septum
3. endocardial cushions spearates atria from ventricles and ads to membranous interventricular septum

path from improper neural crest migration in TPA, or septal defects
Fetal eryhtropoiesis over time
3-8 weeks tolk sac
6-30 weeks liver
9-28 spleen
28+ bone marrow
Vascular post-natal derivatives
umbilical vein- ligamentum teres

umbilical arteries- medial umbilical ligaments
allantois- urachus- median umbilical ligament
ductus arteriosus- ligamentum arteriosum
Findings in neural tube defects, when does error occur?
Occurs in failure to fuse in 4th week

elevated AFP + acetylcholinesterase in CSF
Embryonic brain structures
prosencephalon - leads to telenchepahlon and dienchepalon- becomes cerebrum and thalamus

mesenchephalon becomes the midbrain

rhombencephalon- metenechphalon -> pons and cerebellum

myelenchephalon leads to medulla
Chiari II
cerebellar tonsillar herniation tough formaen magnum with aqueducatla stejosis and hydrocephally

Dandy-Walker- large posterior fossa, cystic enlargement of 4th ventricle, ydrocephalus and spina bifida
Syringomyelia
enlargement of the central spinal cord canal, causes Cape-like bilateral loss of pain and temp sensation in upper extremities C8-T1 typically
Aortic arches and later structures
1st- maxillary artery

3rd- common carotid and proximal pary of internal

4th left, aortic arch, right, right subclavian

6th- pulmonary arteries
Branchial pouch malformation of 3rd and 4th pouches?
DiGeorge- thymic aplasia and hypocalcemia

MEN2A- adrenal medulla, parathyroid 3rd/4th pharyngeal puch, parafolliclar cells derived from neural crest cells, assoicated with 4th/5th pharyngeal pouches
Gastroschisis vs. omphalocele
gastroschisis- not covered by peritoneum

imphalocele organs covered by peritoneum
Duodenal atresia assoiated with
trisomy 21
What happens at 6th and 10th week in abdominal development?
6th- herniation of midgut through umbilicus

10th- returns to abdomen rotating about superior mesennteric artery
Potter's syndrome
bilateral renal agenesis leading to oligohydramins, limb deformites, facial deformities and pulmonary hypoplasia
Horshoe kidney assoicated with
turner syndrome, still have normal kidney functin, trapped under inferior mesenteric artery
Mullerian inhibitory factory
produced by sertoli cells and suppresses paramesonpehric ducts, androgens from leydig cells lead to develoment of mesonephric ducts

mesonephric- becomes seminal vesicles, epipdysmius, ductus eferens, ejac duct
What happens if there are no Sertoli cells?

What happens in 5 alpha reductase deificency?
no sertoli stalles- no antimullerian hromone, both male and femal internal genitalia, male external genitalia

5a reductase deficit- male internal genitalia, ambiguous external, can't produce DHT which develops male external genitalia
Gubernaculum in females and males. What is it's fate?
ovarian ligament/round ligament of uterus

anchors testes within scrotum