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108 Cards in this Set
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Fetal Landmark: Day 0
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Fertilization by sperm forming zygote, initiating embryogenesis
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Fetal Landmark: Day 3
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Morula
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Fetal Landmark: Day 5
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Blastocysts
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Fetal Landmark: Day 6
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Implantation
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Fetal Landmark: within week 2
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Bilaminar disk (epiblast and hypoblast)
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Fetal landmark: within week 3
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Gastrulation - establishes 3 germ layers
Primitive streak Notochord and neural plate begin to form |
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Fetal landmark: week 3-8
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Neural tube formed
Organogenesis Extremely susceptible to teratogens |
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Fetal Landmark: Week 4
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heart begins to beat
upper and lower limb buds begin to form |
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Fetal Landmark: Week 8
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Fetal movement; fetus looks like a baby
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Fetal landmark: week 10
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Genitalia have male/female characteristics
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Alar plate (dorsal)
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Sensory
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Basal plate (ventral)
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Motor
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Rule of 2's for 2nd week
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2 germ layers (bilaminar disk)
2 cavities: amniotic cavity and yolk sac 2 components to the placenta: cytotrophoblast and syncytiotrophoblast |
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Rule of 3's for 3rd week
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3 germ layers (gatrula): ectoderm, mesoderm, and endoderm
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Rule of 4's for 4th week
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4 heart chambers
4 limb buds grow |
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Surface ectoderm
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Adenohypophysis; lens of eye; epithelial linings of skin, ear, eye, and nose; epidermis
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Surface ectoderm
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Adenohypophysis; lens of eye; epithelial linings of skin, ear, eye, and nose; epidermis
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Neuroectoderm
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Neurohypophysis, CNS neurons, oligodendrocytes, astrocytes, ependymal cells, pineal gland
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Neural crest
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ANS, dorsal root ganglia, melanocytes, chromaffin cells of adrenal medulla, enterochromaffin cell, pia and arachnoid, celiac ganglion, Schwann cells, odontoblasts, parafollicular (C) cells of thyroid, laryngeal cartilage, bones of the skull
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Endoderm
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Gut tube epithelium and derivatives (ie. lungs, liver, pancreas, thymus, parathyroid, thyroid, follicular cells)
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Mesoderm
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Dura mater, connective tissue, muscle, bone, cardiovascular structures, lymphatics, blood, urogenital structures, serous linings of body cavities (peritoneal) spleen, adrenal cortex, and kidneys
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Mesodermal defects = VACTERL = Caudal Dysplasia
V: Vertebral defect A: Anal atresia C: cardiac defect T: tracheo-espophageal fistula R: renal defects L: limb defects (bone and muscle) |
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Teratogen: ACE inhibitors
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Renal Damage
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Teratogen: Cocaine
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Abnormal fetal development and fetal addiction
(Placental abruption) |
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Teratogen: Diethylstilbestrol (DES)
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Vaginal clear cell adenocarcinoma
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Teratogen: Iodide
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Congenital goiter of hypothyroidism
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Teratogen: Vitamin A
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extremely high risk for birth defects
(retinoic acid derivative) |
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Teratogen: Thalidomide
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Limb defects (flipper limbs)
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Teratogen: Tobacco
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Preterm labor, placental problems, ADHD
(Hypoxia- decrease uterine blood flow) |
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Teratogen: Warfarin, x-rays, and anticonvulsants
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Multiple anomalies
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Fetal alcohol syndrome
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Leading cause of congenital malformations in US. Newborns have an increased incidence of pre and postnatal development retardation, microcephaly, facial abnormalities, limb dislocation, and heart and lung fistulas.
* Mechanism may be decrease or inhibition of cellular migration |
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Monozygotic twins
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1 zygote splits evenly to develop 2 amniotic sacs within a single common chorion and placenta
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Dizygotic or monozygotic
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Monozygotes taht split early develop 2 placentas, chorions, and amniotic sacs.
Dizygotic develop individual placentas, chorions, and amniotic sacs |
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Placental development
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primary site of nutrient and gas exchange between mother and fetus
*Fetal: Cytotrophoblast composes the inner layer of chorionic villi. Syncytiotrophoblast is the outer layer and secretes hCG Maternal: Decidua basalis derived from endometrium |
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Umbilical cord
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Contains 2 umbilical arteries, which return deoxygenated blood from fetal internal iliac arteries, and 1 umbilical vein, with supplies oxygenated blood from the placenta to the fetus
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A single umbilical artery is associated with congenital and chromosomal abnormalities
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urachus
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removes nitrogenous wastes from fetal bladder (like urethra)
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urachus connects fetal bladder with allantois. Umbilical arteries and veins are derived from the allantois
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What does the Truncus arteriosus (TA) become?
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Ascending aorta and pulmonary trunk
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What does the Bulbus cordis become?
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Smooth pars of the left and right ventricle.
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What does the Primitive ventricle become?
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Trabeculated parts of the left and right ventricle
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What does the primitive atria become?
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Trabeculated left and right atrium
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What does the left horn of sinus venous become?
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Coronary sinus
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What does the right horn of the Sinus venous become?
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Smooth pars of right atrium
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What does the right common cardinal vein and right anterior cardinal vein become?
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SVC
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Development of the Interventricular septum
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1. Muscular ventricular septum froms. Opening is called the interventricular foramen.
2. The aorticopulmonary septum divides the truncus arteriosis into the aortic and pulmonary trunks. 3. The aorticopulmonary septum meets and fuses with the muscular ventricular septum to form the membranous interventricular septum, closing the interventricular foramen |
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Interatrial septum development
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1. Foramen primum narrows as the septum primum grows toward the endocardial cushion
2. Perforations in the septum primum form the foramen secundum as the foramen primum disappears 3.forman secundum maintains the right to left shunt as the septum secundum begins to grow 4.The septum secundum contains the opening (foramen ovale) 5. The foramen secundum enlarges and the upper part of the septum primum degenerates 6. the remaining septum primum is now called the valve of the formen ovale |
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Fetal erythropoiesis occurs in:
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1. yolk sac: (3-8 weeks)
2. liver (6-30 wks) 3. Spleen (9 - 28 wks) 4. Bone marrow (28 wks - +) |
Young Liver Synthesizes Blood
fetal hemoglobin: alpha and gamma adult: alpha and beta |
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In fetal circulation, do the umbilical veins or umbilical arteries have high O2 content?
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Blood in umbilical vein is 80% saturated with O2. Umbilical arteries have low O2 saturation
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The Three important shunts in fetal circulation?
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1. Ductus venosus- blood entering the fetus through the umbilical vein is conducted via the DV into the IVC
2. Foramen ovale- most oxygenated blood reaching the heart via the IVC is diverted through the FO and pumped out the aorta to the head and body 3. Ductus arteriosus- deoxygenated blood from the SVC is expelled into the pulmonary artery and DA to the lower body of the fetus |
at birth, the first breath dec. resistance in pulmonary vasculature causing increase left atrial pressure vs. right atrial pressure-foramen ovale closes = fossa ovalis
- increase O2 leads to decrease in prostaglandins, causing closure of ductus arteriosus |
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what does the umbilical vein become?
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ligamentum teres hepatis
(contained to the falciform ligament) |
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What does the umbilical arteries become?
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the medial umbilical ligament
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What does the ductus arteriosus become?
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ligamentum arteriosum
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What does the ductus venosus become?
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ligamentum venosum
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What dose the foramen ovale become?
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fossa ovalis
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What does the allantois become?
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The urachus- median umbilical ligament
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what does the notochord become?
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nucleus pulposus of intervertebral disk
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1st Aortic Arch derivative?
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part of the MAXillary artery
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First arch is MAXimal
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The derivative of the 2nd aortic arch?
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Stapedial artery and hyoid artery
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Second = Stapedial
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The derivative of the third aortic arch?
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common Carotid artery and proximal part of internal carotid artery
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C is the third letter in the alphabet
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The derivative of the 4th aortic arch?
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on left, aortic arch, on right, proximal part of right subclavian artery
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4th arch - 4 limbs - systemic
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The derivative of the 6th aortic arch?
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proximal part of pulmonary arteries and (on left only) ductus arteriosus
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6th arch = pulmonary and the pulmonary to systemic shunt (DA)
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What composes the brachial (pharyngeal) apparatus?
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brachail clefts, arches, and pouches
Clefts = ectoderm arches - mesoderm pouches = endoderm |
CAP - Cleft/Arch/ Pouch
Ecto/Meso/Endo *Clefts also called grooves |
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Brachial arch 1 derivatives?
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Meckel's cartilage
Manible Malleus and incus sphenoMandibular ligament Muscles of Mastication Mylohyoid and anterior belly of digastric, tensor tympani, tensor veli palantini, anterior 2/3 of the tongue. NERVES: CN V2 and V3 |
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What are the muscles of mastication?
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termporalis, Masseter, later and medial pterygoids
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Derivatives of brachial arch 2
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Reichert's cartilage, Stapes, Styloid process, lesser horn of hyoid, Stylohyoid ligament
Muscles of facial expression, Stapedius, Stylohyoid, posterior belly of digastric NERVE: CN VII |
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Brachial arch 3 derivatives
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Cartilage: greater horn of hyoid
Muscle: stylopharyngeus Nerve: CN IX |
Think of pharynx:
stylopharyngeus innervated by glossopharyngeal nerve |
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Brachial arch 4- 6 derivatives
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Cartilages: thyroid, cricoid, arytenoids, corniculate, cuneiform
Muscles (4th): most of pharyngeal constrictors, cricothyroid, levator veli palantini 6th: all intrinsic muscles of the larynx expcept cricothyroid NERVE: 4- CN X - superior laryngeal branch 6- CNX - recurrent laryngeal branch |
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Brachial arch innervations
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1: CNV2 and CNV3
2: CNVII 3: CNIX 4: CNX 6: CNX |
These cranial nerves are the only ones with both a sensory and motor component (except V2)
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Brachial cleft derivatives
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1st cleft = external auditory meatus
2-4th clefts = temporary cervical sinuses, which are obliterated by the proliferations of 2nd arch mesenchyme |
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1st Brachial pouch
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develops into middle ear cavity; eustachian tube, and mastoid air cells
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1st pouch contributes to endoderm-lined structures of the ear
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2nd brachial pouch
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develops into epithelial lining of palatine tonsil
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3rd brachial pouch
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(dorsal wing) develops into inferior parathyroids
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contributes to 3 structures (thymus, left and right inferior parathyroids)
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3rd brachial pouch (ventral wings)
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develop into thymus
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4th brachial pouch
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(dorsal wing) develops into superior parathyroids
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Aberrant development of 3rd and 4th pouches leads to what problems
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1. DiGeorge syndrome
2.leads to T-cell deficiency (thymic aplasia) 3. hypocalcemia (failure of parathyroid development) |
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Ear Development
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Bones: Malleus, Incus, Stapes
Muscles: Tensor Tympani (V3) Stapedius (VII) Origin: 1st and 2nd arch, 1st cleft, and 1st brachial membrane |
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Tongue development
anterior 2/3 of tongue |
1st brachial arch forms anterior 2/3 of tongue
Sensation: CNV3 Taste: CNVII |
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Tongue Development
posterior 1/3 of tongue |
3rd and 4th arches form the posterior 1/3
Sensation and taste: CNIX Extreme posterior: CN X |
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Motor innervation of tongue
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CN XII
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Innervation for taste
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CN VII, IX, X
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Innervation for pain in the tongue
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CN V3, IX, X
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Thyroid Development
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Thyroid diverticulum arises from the floor of primitive pharynx, descends into neck, thyroglossal duct connects the two. The foramen cecum is the normal remnant of the thyroglossal duct.
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Most common ectopic thyroid tissue site is the tongue
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Cleft Lip
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failure of fusion of the maxillary and medial nasal process (formation of primary palate)
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Cleft Palate
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failure of fusion of the lateral palatine processes, the nasal septum, and/or the median palatine process (formation of secondary palate)
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What is the diaphragm derived from?
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1. Septum transversum
2. Pleuroperitoneal folds 3. Body Wall 4. Dorsal mesentery of esophagus |
Several Parts Build Diaphragm
Diaphragm descends during development so its innervation comes from above (C3,4,5 Keep the Diaphragm alive) |
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Where is the pancreas derived from?
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Pancreas is derived from the foregut. Ventral pancreatic bud becomes the pancreatic head, unicinate process (lower half of head), and main pancreatic duct. Dorsal pancreatic bud becomes the body, tail, isthmus, and accessory pancreatic duct.
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Annular pancreas
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ventral pancreatic bud abnormally encircles 2nd part of the duodenum- forming a rind of pancreatic tissue that may cause duodenal narrowing
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What is the spleen derived from?
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Spleen arises from the dorsal mesentery but is supplied by artery of foregut.
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Where are the distinctions between foregut/midgut/hindgut?
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Foregut- pharynx to duodenum
Midgut- duodenum to transverse colon Hindgut- distal transverse colon to rectum |
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Gastroschisis
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failure of lateral body folds to fuse
extrusion of abdominal contents through abdominal folds |
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Omphalocele
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persistence of herniation of abdominal contents into umbilical cord
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The 4 stages of kidney development?
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1. Pronephros- week 4; then degenerates
2. Mesonephros - function as interim kidney for 1st trimester- later contributes to male genital system 3. Metanephos- permanent 4. Urogenital sinus- develops into bladder, urethra, and allantois |
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Female genital development?
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Default development. Mesonephric duct disappears and paramesonephric duct develops
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Male genital development?
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SRY gene on Y chromosome codes for testis-determining factor. Mullerian inhibiting substance secreted by the testes suppresses development of paramesonephric ducts. Increase androgens - development of mesonephric ducts
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Mesonephric (Wolffian) Duct
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Develops into Male internal structures (except prostate) - Seminal vesicles, Epididymis, Ejaculatory duct, and Ductus deferens
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SEED
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Paramesonephric (Mullerian) Duct
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Develops into fallopian tube, uterus, and part of the vagina.
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What does the genital tubercle become in males? females?
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Dihydrotestosterone- Glans penis
Estrogen- Glans clitoris |
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What does the urogenital sinus become in males? females?
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Dihydrotestosterone- Corpus spongiosum, Bulbourethral glands, and prostate gland
Estrogen-Vestibular bulbs, Greater vestibular glands (Bartholin), Urethral and paraurethral glands (Skene) |
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What does the urogenital folds becomes in males? females?
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Dihydrotestosterone- ventral shaft of penis (penile urethra)
Estrogen- Labia minora |
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What does the Labioscrotal swellings become in males? females?
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Dihydrotestosterone- Scrotum
Estrogen- Labia Majora |
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What are the 3 factors need to develop male gonads?
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1) Sry gene (TDF on the Y chromosome)
2) Testosterone - secreted by the Leydig cells 3) Mullerian- inhibiting factor - secreted by the Sertoli cells |
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Where do the primordial germ cells arise from?
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The wall of the yolk sac
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What is the most common form of ectopic pregnancy?
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Ectopic tubal pregnancy
- the blastocyst implants within the ampulla of the uterine tube because of delayed transport *Risk factors: endometriosis, PID, tubular pelvic surgery, or exposure to diethylstilbestrol |
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Clinical signs of Ectopic tubal pregnancy?
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1)abnormal or brisk uterine bleeding
2) sudden onset of abdominal pain (can be confused with appendicitis) 3) last menses 60 days ago 4) + hCG 5) interperitoneal blood |
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Most come site for ectopic abdominal pregnancy?
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rectouterine pouch (pouch of Douglas).
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Human Chorionic Gonadotropin
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hCG is a glycoprotein - produced by the syncytiotrophoblast
*stimulates the production of progesterone by the corpus lutem to maintain uterine lining |
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What day can hCG be detected in the blood? the urine?
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Blood- Day 8
Urine- Day 10 |
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What can either low or high levels of hCG indicate?
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low levels- spontaneous abortion or ectopic pregnancy
high levels- multiple pregnancies, hydatidiform mole, or gestational trophoblastic neoplasia |
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What is a hydatidiform mole?
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a blighted blastocyst (the embryo dies) followed by a hyperplastic proliferation of the trophoblast within the uterine wall
*clinical signs: preclampsia during the 1st trimester, high levels of hCG, and enlarged uterus with bleeding * 5% of moles develop into gestational trophoblastic neoplasia |
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What is gestational trophoblastic neoplasia?
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a maltignant tumor of the trophoblast that may occur after a normal pregnancy, abortion, or hydatidiform mole. High levels of hCG are clinical significant
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