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71 Cards in this Set

  • Front
  • Back
Factors involved in development of the testes
Sry gene on Y chromosome encodes testes-determining factor (TDF); testosterone by the Leydig cells; Mullerian-inhibiting factor by Sertoli cells.
Describe spermatogenesis
Dormant primordial germ cells differentiate into type A stem cell spermatogonia in puberty; some type A spermatogonia differentiate into type B which enter meiosis; primary and secondary spermatocytes and spermatids are formed; spermatids mature into sperm.
Describe oogenesis
Primordial germ cells differentiate into oogonia in the 4th week; by 5 months all oogonia enter meiosis I forming primary oocytes that remain arrested in prophase of meiosis I until puberty; at puberty, a primary oocyte completes meiosis I; secondary oocyte becomes arrested in metaphase of meiosis II and ovulation occurs; following fertilization in the fallopian tube, secondary oocyte completes meiosis II forming a mature oocyte and a polar body.
Ectopic pregnancy
Risk factors are endometriosis, PID, tubular pelvic surgery. Uterine bleeding, abdominal pain, last menses 60 days ago, hCG+, culdocentesis shows intraperitonial blood.
Blastula
Less than 32 cells beginning on day 2.
Morula
32 cells on day 4
Where does fertilization occur?
Ampulla of fallopian tube
Blastocyst
When fluid secreted within the morula forms the blastocyst cavity on day 5. Inner cells is embryoblast (embryo), outer cells are trophoblast/placenta
Implantation
Occurs on day 6 on the posterior wall of the uterus which is in progestational phase.
Bilaminar embryonic disk
Epiblast and hypoblast form during second week from differentiation of embryoblast.
Changes during second week
Bilaminar embryonic disk forms; amniotic cavity and yolk sac form. Syncytiotrophoblast grows into endometrium reaching blood vessels.
hCG
Produced by syncytiotrophoblast stimulates progesterone production by corpus luteum. Important until week 8 when placenta produces progesterone.
Extraembryonic mesoderm
Derived from epiblast during 2nd week. Extrambryonic somatic mesoderm lines cytotrophoblast and forms connecting stalk. Extraembryonic visceral mesoderm covers the yolk sac.
Hidatiform mole
Blastocyst without embryo. Trophoblast continues to insert itself in uterus. Preeclampsia during 1st trimester, high hCG (>100,000), enlarged uterus and bleeding.
Choriocarcinoma
Malignant trophoblast tumor. Very high levels of hCG. Metastasizes to liver or brain.
Sacrococcygeal teratoma
Tumor arises from remnants of primitive streak and contains various types of tissue
Gastrulation
Week 3. Primitive streak forms within epiblast; Epiblast becomes ectoderm and gives rise to neuroectoderm and neural crest; Hypoblast becomes mesoderm and gives rise to paraxial mesoderm (35 pairs of somites), intermediate and lateral mesoderm; Epiblastic cells migrate through primitive streak to form endoderm between ecto and mesoderm
Acrosomal reaction
Spermal enzymes are released to allow penetration of zona radiata and zona pellucida.
Placenta previa
Placenta attaches to lower uterus. Uterine vessels rupture with profuse bright red bleeding.
Tracheoesophageal fistula
Blind esophagus is MCC. Polyhydramnios, gagging, cyanosis, reflux aspiration and pneumonitis.
Respiratory distress syndrome and hyaline membrane
Lack of surfactant in premature babies and products of diabetic mothers. Dyspnea, tachypnea, nasal flaring and cyanosis. Lecithin:sphyngomyelin < 2. Rx.: surfactant and dexamethasone
Lung development: glandular stage
Weeks 5-17. Respiration not possible.
Lung development: canalicular stage
Weeks 13-25. Respiration not possible. Premature fetuses rarely survive.
Lung development: terminal sac stage
Weeks 24-birth. Type I and II pneumocytes present, respiration possible. Premature fetuses born between weeks 25-28 survive in intensive care,
Lung development: alveolar stage
Birth-8 years. Respiratory bronchioles, terminal sacs, alveolar ducts and alveoli increase in number.
Embryonic heart dilation: truncus arteriosus
Develops into aorta and pulmonary trunk
Embryonic heart dilation: bulbus cordis
Develops into the smooth part of right and left ventricles
Embryonic heart dilation: primitive ventricle
Develops into trabeculated parts of right and left ventricles
Embryonic heart dilation: primitive atrium
Develops into trabeculated parts of right and left atria
Embryonic heart dilation: sinus venosus
Develops into smooth part of right atrium, left coronary sinus and oblique vein of left atrium
Development of aorticopulmonary septum
Neural crest cell origin. Elongate with spiral rotation and divides truncus arteriosus into aorta and pulmonary trunk
Transposition of the great vessels
Neural crest cells fail to spiral rotate. Aorta will be in right ventricle, pulmonary artery in left ventricle. Right to left shunt with early cyanosis. ASD, VSD or PDA are protective.
Tetrallogy of Fallot
Neural crest cells migrate improperly to truncus arteriosus causing pulmonary stenosis, right ventricular hypertrophy, overiding aorta, VSD. Right to left shunt with early cyanosis. Severity of pulmonary stenosis is prognostic.
Persistent truncus arteriosus
Neural crest cells migrate incompletely with only partial formation of AV septum. Right to left shunt with early cyanosis.
Development of the atrial septum
The septum primum grows towards AV septum temporarily forming foramen primum. SP fuses with AV septum obliterating FP. The foramen secundum opens up within SP. Septum secundum forms to the right of the SP forming foramen ovale through which oxygenated blood from inferior vena cava is shunted during fetal life. After birth SP and SS fuse to form atrial septum. Excesive resorption of SP or SS leads to ASD.
Development of interventricular septum
Muscular IV septum grows from the floor towards AV cushions forming foramen ovale. The membranous IV septum closes formamen ovale by the fusion of right bulbar ridge, left bulbar ridge and AV cushinons. Failure of right bulbar ridge, left bulbar ridge and AV cusions tu fuse lead to a membranous ventricular septal defect.
Development of the primitive gut tube
Its formed by incorporation of the yolk sac into the embryo. Epithelial lining and glands of mucosa are from the endoderm. Lamina propria, muscularis mucosae, submucosa, muscularis externa and adventitia are from the mesoderm.
Pyloric stenosis
Hypertrophy of the muscularis externa closes the pylorus. Projectile nonbilious vomiting and small knot at the right costal margin.
Extrahepatic biliary atresia
Lumen of biliary ducts fail to recanalize and are occluded. Jaundice, white-colored stools, dark urine.
Annular pancreas
The ventral and dorsal pancreatic buds form a ring around duodenum causing obstruction.
Duodenal atresia
Lumen of duodenum fails to recanalize and is occluded. Polyhydramnios, bile vomit, distended stomach.
Omphalocele
Midgut loop fails to return to the abdominal cavity forming light gray shiny sac at the ombilical cord filled with loops of small intestine
Ileal Meckel diverticulum
Remnant of vitelline duct that forms a blind pouch on the antimesenteric border of ileum. Could produce inflammation and ulceration or bleeding with iron deficiency anemia.
Vitelline fistula
Vitelline duct persists forming a fistula between the intestinal lumen and the outside of the body at the umbilicus. Drainage of meconium from umbilicus.
Malrotation of the midgut
Partial rotation results in abnormal position of viscera. Associated with volvulus.
Colonic aganglionosis (Hirchsprung)
Failure of the neural crest to form myenteric plexus in sigmoid and rectum. Loss of peristalsis, constipation, obstipation, abdominal distention, dilation of proximal colon, delayed pasage of meconium.
Development of the liver
Hepatic diverticulum evaginates from endoderm of foregut at second portion of duodenum, enters mesentery. Distal part becomes liver and gallbladder, proximal part becomes biliary ducts. Mesentery between liver and gut becomes lesser omentum and between liver and ventral body wall it becomes falciform ligament.
Development of the pancreas
Two pancreatic buds evaginate from foregut endoderm at second portion of duodenum. The dorsal bud grows into dorsal mesentery and forms duct of Santorini, neck, body and tail. The ventral bud rotates around gut tube and enters dorsal mesentery forming duct of Wirsung and inferior head of pancreas.
Development of the spleen
Originates from cells of mesentery behind the stomach. Mesentery around spleen becomes visceral peritoneum of spleen and mesentery between spleen and gut forms gastrosplenic ligament. Mesentery between the spleen and dorsal body wall becomes splenorenal ligament and parietal peritoneum.
Rotations of the gut
Foregut rotates 90 degrees such that dorsal side and spleen rotate to the left and lesser omentum and liver to the right. Midgut herniates out into umbilical cord and rotates 270 degrees around anteroposterior axis.
Development of the pronephros
Appear in week 4 at the cervical intermediate mesoderm. Dissappears at the wend of the 4th week.
Development of the mesonephros
Appear in week 5 at the throracic and lumbar intermediate mesoderm. The medial end forms Bowman's capsule and tubules. The lateral end open into mesonephric Wolffian duct. Mesonephros regresses in the third month. Wolffian ducts persist and form male structures.
Metanephros
The ureteric bud evaginates from the mesonephric duct and forms the collecting ducts, minor calyx, major calyx, renal pelvis and ureter as it penetrates and induces the metanehpric mass. The metanephric mass is an evagination from lumbar intermediate mesoderm and will differentiate into Bowman's capsule and tubules.
Mesonephric Wolffian ducts
Develop into ductus epididymidis, ductus deferens and ejaculatory duct
Urorectal septum
Divides the cloaca into the anorectal canal and the urogenital sinus by week 7
Development of the bladder
The bladder derives from the upper part of the urogenital sinus and is initially continuous with the allantois (which becomes obliterated). The mesonephric duct enters the dorsal bladder wall. The inner epithelium of the bladder is from the endoderm. The smooth muscle is from splachnic mesoderm.
Allantois
Duct initially continuous with urogenital sinus and bladder, becomes an obliterated fibrous urachus (or median umbilical ligament) which connects the apex of the bladder to the umbilicus.
Development of male urethra
Prostatic, membranous and proximal penile urethra develop from lower end of urogenital sinus. Distal penile urethra is derived from the ectodermal cells of the glans penis.
Development of the female urethra
The upper 2/3 from mesonephric ducts and lower 1/3 from the urogenital sinus.
Renal agenesis
Failure of one or both kidneys to develop due to early degeneration of ureteric bud.
Renal cysts or polycystic kidney disease
Abdominal mass, flank pain and hematuria later in life. Associated with cysts of the liver, pancreas and lungs.
Horseshoe kidney
Fusion of both kidneys at inferior poles. Gets trapped behind inferior mesenteric artery as it ascends.
Double ureter
Caused by splitting of ureteric bud. Urine dribbles out and result in incontinence.
Patent urachus
No obliteration of allantois. May cause drainage of urine through umbilicus in patients with obstruction of prostatic urethra or prostatic hyperplasia.
Female pseudohermaphrodite
46XX, ovarian tissues, masculinization of external genitalia. Due to congenital adrenal hyperplasia.
Male pseudohermaphrodite
46XY, testicular tissue, stunted genitalia development. Due to low testosterone (5 alfa-reductase deficiency), low Mullerian inhibiting factor or insensitivity to androgens.
5 alfa reductase deficiency
No conversion of testosterone to dihydrotestosterone. Underdevelopment of penis and scrotum.
Complete androgen insensitivity
46XY with female external genitalia. Mutation in androgen receptor gene.
Hypospadias
Uretheral folds fail to fuse and urethral orifice opens into ventral surface of penis.
Epispadias
Urethral orifice opens into dorsal surface of the penis.
Cryptorchidia
Testes fail to descend within 3 months of birth and may result in infertility