Gestationaltrophoblasticdiseasethis appearsas multipletiny clustersof grape likeechoesmeconiumperitonitisthis is caused byfetal intestinalperforation andthought to berelated to cysticfibrosisDermoidwhat is themost commonbenign germcell tumor ofthe ovaryRockerbottomfootwhat anomalyconsists of a dorsaland lateraldislocation of thetalonavicular jointand a prominentcalcaneus with aconvex rounded soleSpinaBifidaPPT17Micromeliawhat type ofcongenital limbshorteningeffects the proxand distportionsAsherman'sPPT7TOAA patient presentswith a fever andultrasound finds afocal fluid collectionthat involves thefallopian tube, ovaryand cul de sac.HoloprosencephalyThisabnormalityresults from theabnormalcleavage of theprosencephalonsubmucosalwhat type offibroid will mostlikely causeirregular uterinebleedingAmnioticBandSyndromePPT18.2MaternalHTNThis is definedas a bloodpressuremeasuring140/90 orhigherLimb-body wallcomplexthis lethal congenitalabdominal wall defectis characterized byabsent umb cord,exteriorization of abdcontents that attachto the placentaOmphalocelemidline gutherniationwith acoveringmembranePseudomyoxomaPeritoneiPPT13MissedAbortionPPT2CystPPT1MaturecysticteratomaPPT9NuchalTranslucenyPPT5subchorionichemorrhagePPT4completeatrioventricularseptal defectthis is a largeventricular andatrial septaldefect with asingle freefloating leafletUreteropelvicJunctionUPJWhat is themost commonsite forobstruction inthe fetal urinarybladderCompletePlacentaPreviaPPT14pulmonarysequestrationPPT16MucinouscystadenocarcinomaPPT12OvarianTorsionPPT11CysticAdenomatoidMalformationwhat lungabnormality ischaracterized bythe replacementof normal tissuewith cystic tissueNuchalFoldPPT15GastrochisisThis abdominaldefect istypically locatedto the RT of theumbilicusRhizomeliacongenital limbshortening ofthe proxsegment of theext is calledHydranencephalywhat condition canbe acquired from apossible vascularaccident or antenatalinfections causing thecerebral hemisperesto be replaced w/fluidPCOSPPT10Meckel-GruberSyndromeencephalocele,polydactyly, bilrenal cysts,+severe oligo areassociatedw/what syndromeMacrosomicA fetus isconsidered thisif they measuregreater than4000 gramsand the 90th %CaudalregressionsyndromeWhat syndrome isassociated with thesefindings: GI and GUabnormalities,abnormaldevelopment of lowerspine, and sacralagenesisCloacalexstrophyIf a mass is seenbetween the fetallegs, but notbladder is seen,the mass is mostlikelyClubfootTalipesequinovarusis thetechnicalterm forgameteintrafallopiantube transferthis procedureplacesharvested eggsand sperm intothe fallopiantubeCysticHygromathis is causedby amalformation ofthe lymphaticsystemDuodenalAtresiaPPT15AdenomyosisPPT6MeigsSyndromethe triad ofascites, pleuraleffusion, andbenign ovarianfibroma iscalledFitz-HughCurtisWhatsyndrome ischaracterizedby perihepaticinflammationplacentaaccretathis is thegrowth ofchorionic villisuperficiallyinto themyometriumEbstein'sAnomalyin this anomalythe tricuspidvalve isabnormallyplaced inferiorlyMonoamnioticThis type oftwin pregnancycarries up to a50% chance ofdeathpartialmolePPT3Turner'sSyndromePPT18Gestationaltrophoblasticdiseasethis appearsas multipletiny clustersof grape likeechoesmeconiumperitonitisthis is caused byfetal intestinalperforation andthought to berelated to cysticfibrosisDermoidwhat is themost commonbenign germcell tumor ofthe ovaryRockerbottomfootwhat anomalyconsists of a dorsaland lateraldislocation of thetalonavicular jointand a prominentcalcaneus with aconvex rounded soleSpinaBifidaPPT17Micromeliawhat type ofcongenital limbshorteningeffects the proxand distportionsAsherman'sPPT7TOAA patient presentswith a fever andultrasound finds afocal fluid collectionthat involves thefallopian tube, ovaryand cul de sac.HoloprosencephalyThisabnormalityresults from theabnormalcleavage of theprosencephalonsubmucosalwhat type offibroid will mostlikely causeirregular uterinebleedingAmnioticBandSyndromePPT18.2MaternalHTNThis is definedas a bloodpressuremeasuring140/90 orhigherLimb-body wallcomplexthis lethal congenitalabdominal wall defectis characterized byabsent umb cord,exteriorization of abdcontents that attachto the placentaOmphalocelemidline gutherniationwith acoveringmembranePseudomyoxomaPeritoneiPPT13MissedAbortionPPT2CystPPT1MaturecysticteratomaPPT9NuchalTranslucenyPPT5subchorionichemorrhagePPT4completeatrioventricularseptal defectthis is a largeventricular andatrial septaldefect with asingle freefloating leafletUreteropelvicJunctionUPJWhat is themost commonsite forobstruction inthe fetal urinarybladderCompletePlacentaPreviaPPT14pulmonarysequestrationPPT16MucinouscystadenocarcinomaPPT12OvarianTorsionPPT11CysticAdenomatoidMalformationwhat lungabnormality ischaracterized bythe replacementof normal tissuewith cystic tissueNuchalFoldPPT15GastrochisisThis abdominaldefect istypically locatedto the RT of theumbilicusRhizomeliacongenital limbshortening ofthe proxsegment of theext is calledHydranencephalywhat condition canbe acquired from apossible vascularaccident or antenatalinfections causing thecerebral hemisperesto be replaced w/fluidPCOSPPT10Meckel-GruberSyndromeencephalocele,polydactyly, bilrenal cysts,+severe oligo areassociatedw/what syndromeMacrosomicA fetus isconsidered thisif they measuregreater than4000 gramsand the 90th %CaudalregressionsyndromeWhat syndrome isassociated with thesefindings: GI and GUabnormalities,abnormaldevelopment of lowerspine, and sacralagenesisCloacalexstrophyIf a mass is seenbetween the fetallegs, but notbladder is seen,the mass is mostlikelyClubfootTalipesequinovarusis thetechnicalterm forgameteintrafallopiantube transferthis procedureplacesharvested eggsand sperm intothe fallopiantubeCysticHygromathis is causedby amalformation ofthe lymphaticsystemDuodenalAtresiaPPT15AdenomyosisPPT6MeigsSyndromethe triad ofascites, pleuraleffusion, andbenign ovarianfibroma iscalledFitz-HughCurtisWhatsyndrome ischaracterizedby perihepaticinflammationplacentaaccretathis is thegrowth ofchorionic villisuperficiallyinto themyometriumEbstein'sAnomalyin this anomalythe tricuspidvalve isabnormallyplaced inferiorlyMonoamnioticThis type oftwin pregnancycarries up to a50% chance ofdeathpartialmolePPT3Turner'sSyndromePPT18

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