21hydroxylaseDeficiency ismostcommoncause ofCAHLuteomaHyperplasticmassof luteinized cells1/3 associatedwith maternalhirsutismor virilization 17 hydroxyprogesteroneLab testused toevaluatefor CAHAlfredJostExperimentswith rabbitsexplained roleof local T inmaledevelopmentWolffianductsMale ductsnamed afterfamousGermanembryologistand anatomistGermcellsA cell thatdevelopsinto areproductivecellPseudogeneCommonmutationin classicCAHVirilizationLoss of femalebody contours,deepeningvoiceclitoromegalyetcDexamethasoneSteroidtreatment hatedby pregnantwomen at riskfor baby withCAHDHTActive formoftestosteroneAdrenalcrisisWhathappens toCAH babyafter deliveryTestosterone19 carbonsteroidconvertedinto DHTGermline stemcellsMice seemto havethese butwe may notSertolicellsCells thatnourishmake germcells intubules6-7millionNumber ofoogonia at20 weeksgestationPara-mesonephrousDescribed byJohannesMuller in1830TruehermaphroditeIndividualwith bothovarian andtesticulartissueherniauterineinguinalesyndromeProbably thediagnosis ofthe Pope inConclave1/6Odds offemaleoffspring ofnormal sisterwill be 46 XYOutercortexConsists ofovarianfollicles andstroma inbetween themAMHTGF-beta familymember thatcausesregressionof mullerianductReteovariiVestigialtubules andLeydig cells inhilarregion of ovary MeiosisProcess bywhichoogoniabecomeoocytes TGF-betasuperfamilyAMH is amember ofthis super-familyY containingIntrabdominalgonadNeedsto beremovedHyperpigmentationFrequentlyseem incasesof high levelsof ACTHMRKHCanpresentsimilar toAISSomaticcellsIn the absenceof ovarian germcells theseovarian cellsfail to developClassicCAHCan haveboth salt-wasting andsimplevirilizing formsVirilizedfemalePreferred overfemalepseudo-hermaphroditeby DrG1-2%enzymeactivityPatients withsimple virilizingmost often havepoint mutationswith ___enzyme activity hCGStimTestcan distinguishbetween 5αreductasedeficiency, defectsin testosteronesynthesis andincomplete AIS 11 betahydroxylaseAccountsfor 5-8%of CAHcasesHermaphroditusIn Greekmythologywas a childof Aphroditeand Hermes.PrincetonDrG almamater andwhere authorof Middlesexwas on facultyACTHIncreasedproduction inpituitary ofCAH babiesCompleteAISfirst describedat Yale whereMorris coinedthe term“testicularfeminization” 6metersLength ofhumanepididymisSaltwastingSpecific formof classicCAH leadingto neonataldeathSimplevirilizingNon-lethalform ofclassicCAHMiddlesexNovel byJeffreyEuginidesCortisolSteroid that isproduced from11-deoxycortisolby 11hydroxylaseLeydigcellsAndrogenproducingcells intestes17hydroxylasedeficiencyrare causeof CAH with~ 100 casesreported GranulosacellsA single layerof these cellsis found inprimordialfollicles1/3Odds thatphenotypicsisters ofaffectedindividualare XYMullerianductsNamed afterfamousembryologistthese ductsdevelop intofemale reproductivesystem PGDCan be usedwith IVF toscreen forCAHThecaluteincysts10-20% inwomen withgestationaltrophoblasticdisease PrimordialfolliclesThe structurethat formswhen anoogoniummatures.HOXGenesControl expressionof growth factorsthat induce thestraight wolffianduct to elongateand coil 5alphareductaseEnzymethatconverts Tto DHTACTHStimtestUsed toscreenfor CAHMesonephrosDescribedby CasparWolff in1759InnermedullaryregionContainsovarianblood vessels,lymphaticvessels,and nerves.PlacentaProtectsCAH fetusprior todeliveryYupicEskimoHighestcarrierfrequencyof CAHRenalsystemAnomalies inthis systemoften found inpatients withmulleriananomaliesMetanephrousDevelopsintothe renalsystemUndervirilizedmalePreferred overmale pseudo-hermaphroditeby DrGOogoniaThesediploid germcells developinto oocytesNomogramUsed tocomparebasal andstim levels of17-OHP20weeksgestationAge withmaximumnumber offemale germcellsSRYRegion of Ychromosomethat leads tomaledevelopmentalpathwayCompoundheterozygoteNon-classicforms of 21Hydroxylasedeficiency areusually thisgenetic mixtureIncompleteAISphenotype ispredominantlyundervirilizedmale withgreat range 21hydroxylaseDeficiency ismostcommoncause ofCAHLuteomaHyperplasticmassof luteinized cells1/3 associatedwith maternalhirsutismor virilization 17 hydroxyprogesteroneLab testused toevaluatefor CAHAlfredJostExperimentswith rabbitsexplained roleof local T inmaledevelopmentWolffianductsMale ductsnamed afterfamousGermanembryologistand anatomistGermcellsA cell thatdevelopsinto areproductivecellPseudogeneCommonmutationin classicCAHVirilizationLoss of femalebody contours,deepeningvoiceclitoromegalyetcDexamethasoneSteroidtreatment hatedby pregnantwomen at riskfor baby withCAHDHTActive formoftestosteroneAdrenalcrisisWhathappens toCAH babyafter deliveryTestosterone19 carbonsteroidconvertedinto DHTGermline stemcellsMice seemto havethese butwe may notSertolicellsCells thatnourishmake germcells intubules6-7millionNumber ofoogonia at20 weeksgestationPara-mesonephrousDescribed byJohannesMuller in1830TruehermaphroditeIndividualwith bothovarian andtesticulartissueherniauterineinguinalesyndromeProbably thediagnosis ofthe Pope inConclave1/6Odds offemaleoffspring ofnormal sisterwill be 46 XYOutercortexConsists ofovarianfollicles andstroma inbetween themAMHTGF-beta familymember thatcausesregressionof mullerianductReteovariiVestigialtubules andLeydig cells inhilarregion of ovary MeiosisProcess bywhichoogoniabecomeoocytes TGF-betasuperfamilyAMH is amember ofthis super-familyY containingIntrabdominalgonadNeedsto beremovedHyperpigmentationFrequentlyseem incasesof high levelsof ACTHMRKHCanpresentsimilar toAISSomaticcellsIn the absenceof ovarian germcells theseovarian cellsfail to developClassicCAHCan haveboth salt-wasting andsimplevirilizing formsVirilizedfemalePreferred overfemalepseudo-hermaphroditeby DrG1-2%enzymeactivityPatients withsimple virilizingmost often havepoint mutationswith ___enzyme activity hCGStimTestcan distinguishbetween 5αreductasedeficiency, defectsin testosteronesynthesis andincomplete AIS 11 betahydroxylaseAccountsfor 5-8%of CAHcasesHermaphroditusIn Greekmythologywas a childof Aphroditeand Hermes.PrincetonDrG almamater andwhere authorof Middlesexwas on facultyACTHIncreasedproduction inpituitary ofCAH babiesCompleteAISfirst describedat Yale whereMorris coinedthe term“testicularfeminization” 6metersLength ofhumanepididymisSaltwastingSpecific formof classicCAH leadingto neonataldeathSimplevirilizingNon-lethalform ofclassicCAHMiddlesexNovel byJeffreyEuginidesCortisolSteroid that isproduced from11-deoxycortisolby 11hydroxylaseLeydigcellsAndrogenproducingcells intestes17hydroxylasedeficiencyrare causeof CAH with~ 100 casesreported GranulosacellsA single layerof these cellsis found inprimordialfollicles1/3Odds thatphenotypicsisters ofaffectedindividualare XYMullerianductsNamed afterfamousembryologistthese ductsdevelop intofemale reproductivesystem PGDCan be usedwith IVF toscreen forCAHThecaluteincysts10-20% inwomen withgestationaltrophoblasticdisease PrimordialfolliclesThe structurethat formswhen anoogoniummatures.HOXGenesControl expressionof growth factorsthat induce thestraight wolffianduct to elongateand coil 5alphareductaseEnzymethatconverts Tto DHTACTHStimtestUsed toscreenfor CAHMesonephrosDescribedby CasparWolff in1759InnermedullaryregionContainsovarianblood vessels,lymphaticvessels,and nerves.PlacentaProtectsCAH fetusprior todeliveryYupicEskimoHighestcarrierfrequencyof CAHRenalsystemAnomalies inthis systemoften found inpatients withmulleriananomaliesMetanephrousDevelopsintothe renalsystemUndervirilizedmalePreferred overmale pseudo-hermaphroditeby DrGOogoniaThesediploid germcells developinto oocytesNomogramUsed tocomparebasal andstim levels of17-OHP20weeksgestationAge withmaximumnumber offemale germcellsSRYRegion of Ychromosomethat leads tomaledevelopmentalpathwayCompoundheterozygoteNon-classicforms of 21Hydroxylasedeficiency areusually thisgenetic mixtureIncompleteAISphenotype ispredominantlyundervirilizedmale withgreat range 

REI DSD Bingo - 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. Deficiency is most common cause of CAH
    21 hydroxylase
  2. Hyperplastic mass of luteinized cells 1/3 associated with maternal hirsutism or virilization
    Luteoma
  3. Lab test used to evaluate for CAH
    17 hydroxy progesterone
  4. Experiments with rabbits explained role of local T in male development
    Alfred Jost
  5. Male ducts named after famous German embryologist and anatomist
    Wolffian ducts
  6. A cell that develops into a reproductive cell
    Germ cells
  7. Common mutation in classic CAH
    Pseudogene
  8. Loss of female body contours, deepening voice clitoromegaly etc
    Virilization
  9. Steroid treatment hated by pregnant women at risk for baby with CAH
    Dexamethasone
  10. Active form of testosterone
    DHT
  11. What happens to CAH baby after delivery
    Adrenal crisis
  12. 19 carbon steroid converted into DHT
    Testosterone
  13. Mice seem to have these but we may not
    Germ line stem cells
  14. Cells that nourish make germ cells in tubules
    Sertoli cells
  15. Number of oogonia at 20 weeks gestation
    6-7 million
  16. Described by Johannes Muller in 1830
    Para-mesonephrous
  17. Individual with both ovarian and testicular tissue
    True hermaphrodite
  18. Probably the diagnosis of the Pope in Conclave
    hernia uterine inguinale syndrome
  19. Odds of female offspring of normal sister will be 46 XY
    1/6
  20. Consists of ovarian follicles and stroma in between them
    Outer cortex
  21. TGF-beta family member that causes regression of mullerian duct
    AMH
  22. Vestigial tubules and Leydig cells in hilar region of ovary
    Rete ovarii
  23. Process by which oogonia become oocytes
    Meiosis
  24. AMH is a member of this super- family
    TGF-beta superfamily
  25. Needs to be removed
    Y containing Intrabdominal gonad
  26. Frequently seem in cases of high levels of ACTH
    Hyper pigmentation
  27. Can present similar to AIS
    MRKH
  28. In the absence of ovarian germ cells these ovarian cells fail to develop
    Somatic cells
  29. Can have both salt-wasting and simple virilizing forms
    Classic CAH
  30. Preferred over female pseudo-hermaphrodite by DrG
    Virilized female
  31. Patients with simple virilizing most often have point mutations with ___ enzyme activity
    1-2% enzyme activity
  32. can distinguish between 5α reductase deficiency, defects in testosterone synthesis and incomplete AIS
    hCG Stim Test
  33. Accounts for 5-8% of CAH cases
    11 beta hydroxylase
  34. In Greek mythology was a child of Aphrodite and Hermes.
    Hermaphroditus
  35. DrG alma mater and where author of Middlesex was on faculty
    Princeton
  36. Increased production in pituitary of CAH babies
    ACTH
  37. first described at Yale where Morris coined the term “testicular feminization”
    Complete AIS
  38. Length of human epididymis
    6 meters
  39. Specific form of classic CAH leading to neonatal death
    Salt wasting
  40. Non-lethal form of classic CAH
    Simple virilizing
  41. Novel by Jeffrey Euginides
    Middlesex
  42. Steroid that is produced from 11-deoxycortisol by 11 hydroxylase
    Cortisol
  43. Androgen producing cells in testes
    Leydig cells
  44. rare cause of CAH with ~ 100 cases reported
    17 hydroxylase deficiency
  45. A single layer of these cells is found in primordial follicles
    Granulosa cells
  46. Odds that phenotypic sisters of affected individual are XY
    1/3
  47. Named after famous embryologist these ducts develop into female reproductive system
    Mullerian ducts
  48. Can be used with IVF to screen for CAH
    PGD
  49. 10-20% in women with gestational trophoblastic disease
    Theca lutein cysts
  50. The structure that forms when an oogonium matures.
    Primordial follicles
  51. Control expression of growth factors that induce the straight wolffian duct to elongate and coil
    HOX Genes
  52. Enzyme that converts T to DHT
    5alpha reductase
  53. Used to screen for CAH
    ACTH Stim test
  54. Described by Caspar Wolff in 1759
    Mesonephros
  55. Contains ovarian blood vessels, lymphatic vessels, and nerves.
    Inner medullary region
  56. Protects CAH fetus prior to delivery
    Placenta
  57. Highest carrier frequency of CAH
    Yupic Eskimo
  58. Anomalies in this system often found in patients with mullerian anomalies
    Renal system
  59. Develops into the renal system
    Metanephrous
  60. Preferred over male pseudo-hermaphrodite by DrG
    Undervirilized male
  61. These diploid germ cells develop into oocytes
    Oogonia
  62. Used to compare basal and stim levels of 17-OHP
    Nomogram
  63. Age with maximum number of female germ cells
    20 weeks gestation
  64. Region of Y chromosome that leads to male developmental pathway
    SRY
  65. Non-classic forms of 21 Hydroxylase deficiency are usually this genetic mixture
    Compound heterozygote
  66. phenotype is predominantly undervirilized male with great range
    Incomplete AIS