Asherman'sPPT7Rockerbottomfootwhat anomalyconsists of a dorsaland lateraldislocation of thetalonavicular jointand a prominentcalcaneus with aconvex rounded soleTOAA patient presentswith a fever andultrasound finds afocal fluid collectionthat involves thefallopian tube, ovaryand cul de sac.OvarianTorsionPPT11Omphalocelemidline gutherniationwith acoveringmembranegameteintrafallopiantube transferthis procedureplacesharvested eggsand sperm intothe fallopiantubeEbstein'sAnomalyin this anomalythe tricuspidvalve isabnormallyplaced inferiorlysubmucosalwhat type offibroid will mostlikely causeirregular uterinebleedingmeconiumperitonitisthis is caused byfetal intestinalperforation andthought to berelated to cysticfibrosisGastrochisisThis abdominaldefect istypically locatedto the RT of theumbilicusSpinaBifidaPPT17UreteropelvicJunctionUPJWhat is themost commonsite forobstruction inthe fetal urinarybladderPseudomyoxomaPeritoneiPPT13pulmonarysequestrationPPT16PCOSPPT10partialmolePPT3Rhizomeliacongenital limbshortening ofthe proxsegment of theext is calledHoloprosencephalyThisabnormalityresults from theabnormalcleavage of theprosencephalonCysticHygromathis is causedby amalformation ofthe lymphaticsystemCloacalexstrophyIf a mass is seenbetween the fetallegs, but notbladder is seen,the mass is mostlikelyMonoamnioticThis type oftwin pregnancycarries up to a50% chance ofdeathCystPPT1CysticAdenomatoidMalformationwhat lungabnormality ischaracterized bythe replacementof normal tissuewith cystic tissueMaternalHTNThis is definedas a bloodpressuremeasuring140/90 orhigherLimb-body wallcomplexthis lethal congenitalabdominal wall defectis characterized byabsent umb cord,exteriorization of abdcontents that attachto the placentaNuchalTranslucenyPPT5placentaaccretathis is thegrowth ofchorionic villisuperficiallyinto themyometriumMacrosomicA fetus isconsidered thisif they measuregreater than4000 gramsand the 90th %ClubfootTalipesequinovarusis thetechnicalterm forMeckel-GruberSyndromeencephalocele,polydactyly, bilrenal cysts,+severe oligo areassociatedw/what syndromeMissedAbortionPPT2Gestationaltrophoblasticdiseasethis appearsas multipletiny clustersof grape likeechoesMicromeliawhat type ofcongenital limbshorteningeffects the proxand distportionsNuchalFoldPPT15Turner'sSyndromePPT18DuodenalAtresiaPPT15Hydranencephalywhat condition canbe acquired from apossible vascularaccident or antenatalinfections causing thecerebral hemisperesto be replaced w/fluidDermoidwhat is themost commonbenign germcell tumor ofthe ovarycompleteatrioventricularseptal defectthis is a largeventricular andatrial septaldefect with asingle freefloating leafletsubchorionichemorrhagePPT4MucinouscystadenocarcinomaPPT12CompletePlacentaPreviaPPT14MaturecysticteratomaPPT9AmnioticBandSyndromePPT18.2MeigsSyndromethe triad ofascites, pleuraleffusion, andbenign ovarianfibroma iscalledFitz-HughCurtisWhatsyndrome ischaracterizedby perihepaticinflammationCaudalregressionsyndromeWhat syndrome isassociated with thesefindings: GI and GUabnormalities,abnormaldevelopment of lowerspine, and sacralagenesisAdenomyosisPPT6Asherman'sPPT7Rockerbottomfootwhat anomalyconsists of a dorsaland lateraldislocation of thetalonavicular jointand a prominentcalcaneus with aconvex rounded soleTOAA patient presentswith a fever andultrasound finds afocal fluid collectionthat involves thefallopian tube, ovaryand cul de sac.OvarianTorsionPPT11Omphalocelemidline gutherniationwith acoveringmembranegameteintrafallopiantube transferthis procedureplacesharvested eggsand sperm intothe fallopiantubeEbstein'sAnomalyin this anomalythe tricuspidvalve isabnormallyplaced inferiorlysubmucosalwhat type offibroid will mostlikely causeirregular uterinebleedingmeconiumperitonitisthis is caused byfetal intestinalperforation andthought to berelated to cysticfibrosisGastrochisisThis abdominaldefect istypically locatedto the RT of theumbilicusSpinaBifidaPPT17UreteropelvicJunctionUPJWhat is themost commonsite forobstruction inthe fetal urinarybladderPseudomyoxomaPeritoneiPPT13pulmonarysequestrationPPT16PCOSPPT10partialmolePPT3Rhizomeliacongenital limbshortening ofthe proxsegment of theext is calledHoloprosencephalyThisabnormalityresults from theabnormalcleavage of theprosencephalonCysticHygromathis is causedby amalformation ofthe lymphaticsystemCloacalexstrophyIf a mass is seenbetween the fetallegs, but notbladder is seen,the mass is mostlikelyMonoamnioticThis type oftwin pregnancycarries up to a50% chance ofdeathCystPPT1CysticAdenomatoidMalformationwhat lungabnormality ischaracterized bythe replacementof normal tissuewith cystic tissueMaternalHTNThis is definedas a bloodpressuremeasuring140/90 orhigherLimb-body wallcomplexthis lethal congenitalabdominal wall defectis characterized byabsent umb cord,exteriorization of abdcontents that attachto the placentaNuchalTranslucenyPPT5placentaaccretathis is thegrowth ofchorionic villisuperficiallyinto themyometriumMacrosomicA fetus isconsidered thisif they measuregreater than4000 gramsand the 90th %ClubfootTalipesequinovarusis thetechnicalterm forMeckel-GruberSyndromeencephalocele,polydactyly, bilrenal cysts,+severe oligo areassociatedw/what syndromeMissedAbortionPPT2Gestationaltrophoblasticdiseasethis appearsas multipletiny clustersof grape likeechoesMicromeliawhat type ofcongenital limbshorteningeffects the proxand distportionsNuchalFoldPPT15Turner'sSyndromePPT18DuodenalAtresiaPPT15Hydranencephalywhat condition canbe acquired from apossible vascularaccident or antenatalinfections causing thecerebral hemisperesto be replaced w/fluidDermoidwhat is themost commonbenign germcell tumor ofthe ovarycompleteatrioventricularseptal defectthis is a largeventricular andatrial septaldefect with asingle freefloating leafletsubchorionichemorrhagePPT4MucinouscystadenocarcinomaPPT12CompletePlacentaPreviaPPT14MaturecysticteratomaPPT9AmnioticBandSyndromePPT18.2MeigsSyndromethe triad ofascites, pleuraleffusion, andbenign ovarianfibroma iscalledFitz-HughCurtisWhatsyndrome ischaracterizedby perihepaticinflammationCaudalregressionsyndromeWhat syndrome isassociated with thesefindings: GI and GUabnormalities,abnormaldevelopment of lowerspine, and sacralagenesisAdenomyosisPPT6

DMSG 415 Final Exam - Call List

(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.


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  1. PPT 7
    Asherman's
  2. what anomaly consists of a dorsal and lateral dislocation of the talonavicular joint and a prominent calcaneus with a convex rounded sole
    Rocker bottom foot
  3. A patient presents with a fever and ultrasound finds a focal fluid collection that involves the fallopian tube, ovary and cul de sac.
    TOA
  4. PPT 11
    Ovarian Torsion
  5. midline gut herniation with a covering membrane
    Omphalocele
  6. this procedure places harvested eggs and sperm into the fallopian tube
    gamete intrafallopian tube transfer
  7. in this anomaly the tricuspid valve is abnormally placed inferiorly
    Ebstein's Anomaly
  8. what type of fibroid will most likely cause irregular uterine bleeding
    submucosal
  9. this is caused by fetal intestinal perforation and thought to be related to cystic fibrosis
    meconium peritonitis
  10. This abdominal defect is typically located to the RT of the umbilicus
    Gastrochisis
  11. PPT 17
    Spina Bifida
  12. What is the most common site for obstruction in the fetal urinary bladder
    Ureteropelvic Junction UPJ
  13. PPT 13
    Pseudomyoxoma Peritonei
  14. PPT 16
    pulmonary sequestration
  15. PPT 10
    PCOS
  16. PPT 3
    partial mole
  17. congenital limb shortening of the prox segment of the ext is called
    Rhizomelia
  18. This abnormality results from the abnormal cleavage of the prosencephalon
    Holoprosencephaly
  19. this is caused by a malformation of the lymphatic system
    Cystic Hygroma
  20. If a mass is seen between the fetal legs, but not bladder is seen, the mass is most likely
    Cloacal exstrophy
  21. This type of twin pregnancy carries up to a 50% chance of death
    Monoamniotic
  22. PPT 1
    Cyst
  23. what lung abnormality is characterized by the replacement of normal tissue with cystic tissue
    Cystic Adenomatoid Malformation
  24. This is defined as a blood pressure measuring 140/90 or higher
    Maternal HTN
  25. this lethal congenital abdominal wall defect is characterized by absent umb cord, exteriorization of abd contents that attach to the placenta
    Limb-body wall complex
  26. PPT 5
    Nuchal Transluceny
  27. this is the growth of chorionic villi superficially into the myometrium
    placenta accreta
  28. A fetus is considered this if they measure greater than 4000 grams and the 90th %
    Macrosomic
  29. Talipes equinovarus is the technical term for
    Clubfoot
  30. encephalocele, polydactyly, bil renal cysts, +severe oligo are associated w/what syndrome
    Meckel-Gruber Syndrome
  31. PPT 2
    Missed Abortion
  32. this appears as multiple tiny clusters of grape like echoes
    Gestational trophoblastic disease
  33. what type of congenital limb shortening effects the prox and dist portions
    Micromelia
  34. PPT 15
    Nuchal Fold
  35. PPT 18
    Turner's Syndrome
  36. PPT 15
    Duodenal Atresia
  37. what condition can be acquired from a possible vascular accident or antenatal infections causing the cerebral hemisperes to be replaced w/fluid
    Hydranencephaly
  38. what is the most common benign germ cell tumor of the ovary
    Dermoid
  39. this is a large ventricular and atrial septal defect with a single free floating leaflet
    complete atrioventricular septal defect
  40. PPT 4
    subchorionic hemorrhage
  41. PPT 12
    Mucinous cystadenocarcinoma
  42. PPT 14
    Complete Placenta Previa
  43. PPT 9
    Mature cystic teratoma
  44. PPT 18.2
    Amniotic Band Syndrome
  45. the triad of ascites, pleural effusion, and benign ovarian fibroma is called
    Meigs Syndrome
  46. What syndrome is characterized by perihepatic inflammation
    Fitz-Hugh Curtis
  47. What syndrome is associated with these findings: GI and GU abnormalities, abnormal development of lower spine, and sacral agenesis
    Caudal regression syndrome
  48. PPT 6
    Adenomyosis