OogoniaThesediploid germcells developinto oocytesACTHIncreasedproduction inpituitary ofCAH babiesMesonephrosDescribedby CasparWolff in1759VirilizedfemalePreferred overfemalepseudo-hermaphroditeby DrGDexamethasoneSteroidtreatment hatedby pregnantwomen at riskfor baby withCAHHOXGenesControl expressionof growth factorsthat induce thestraight wolffianduct to elongateand coil OutercortexConsists ofovarianfollicles andstroma inbetween themClassicCAHCan haveboth salt-wasting andsimplevirilizing formsThecaluteincysts10-20% inwomen withgestationaltrophoblasticdisease RenalsystemAnomalies inthis systemoften found inpatients withmulleriananomaliesPGDCan be usedwith IVF toscreen forCAHLuteomaHyperplasticmassof luteinized cells1/3 associatedwith maternalhirsutismor virilization herniauterineinguinalesyndromeProbably thediagnosis ofthe Pope inConclaveUndervirilizedmalePreferred overmale pseudo-hermaphroditeby DrGHermaphroditusIn Greekmythologywas a childof Aphroditeand Hermes.IncompleteAISphenotype ispredominantlyundervirilizedmale withgreat range SertolicellsCells thatnourishmake germcells intubulesTruehermaphroditeIndividualwith bothovarian andtesticulartissueCortisolSteroid that isproduced from11-deoxycortisolby 11hydroxylase5alphareductaseEnzymethatconverts Tto DHT17hydroxylasedeficiencyrare causeof CAH with~ 100 casesreported 6-7millionNumber ofoogonia at20 weeksgestationSRYRegion of Ychromosomethat leads tomaledevelopmentalpathwayPrimordialfolliclesThe structurethat formswhen anoogoniummatures.InnermedullaryregionContainsovarianblood vessels,lymphaticvessels,and nerves.HyperpigmentationFrequentlyseem incasesof high levelsof ACTHPrincetonDrG almamater andwhere authorof Middlesexwas on faculty21hydroxylaseDeficiency ismostcommoncause ofCAHSimplevirilizingNon-lethalform ofclassicCAHReteovariiVestigialtubules andLeydig cells inhilarregion of ovary PlacentaProtectsCAH fetusprior todeliveryYupicEskimoHighestcarrierfrequencyof CAH1/3Odds thatphenotypicsisters ofaffectedindividualare XYGermline stemcellsMice seemto havethese butwe may notY containingIntrabdominalgonadNeedsto beremovedTestosterone19 carbonsteroidconvertedinto DHTMiddlesexNovel byJeffreyEuginidesCompoundheterozygoteNon-classicforms of 21Hydroxylasedeficiency areusually thisgenetic mixturePseudogeneCommonmutationin classicCAHhCGStimTestcan distinguishbetween 5αreductasedeficiency, defectsin testosteronesynthesis andincomplete AIS 20weeksgestationAge withmaximumnumber offemale germcellsWolffianductsMale ductsnamed afterfamousGermanembryologistand anatomist1/6Odds offemaleoffspring ofnormal sisterwill be 46 XYAlfredJostExperimentswith rabbitsexplained roleof local T inmaledevelopmentSaltwastingSpecific formof classicCAH leadingto neonataldeathSomaticcellsIn the absenceof ovarian germcells theseovarian cellsfail to developTGF-betasuperfamilyAMH is amember ofthis super-family6metersLength ofhumanepididymisVirilizationLoss of femalebody contours,deepeningvoiceclitoromegalyetc17 hydroxyprogesteroneLab testused toevaluatefor CAHLeydigcellsAndrogenproducingcells intestesCompleteAISfirst describedat Yale whereMorris coinedthe term“testicularfeminization” Para-mesonephrousDescribed byJohannesMuller in1830AMHTGF-beta familymember thatcausesregressionof mullerianductNomogramUsed tocomparebasal andstim levels of17-OHPACTHStimtestUsed toscreenfor CAHMetanephrousDevelopsintothe renalsystemMullerianductsNamed afterfamousembryologistthese ductsdevelop intofemale reproductivesystem 1-2%enzymeactivityPatients withsimple virilizingmost often havepoint mutationswith ___enzyme activity GermcellsA cell thatdevelopsinto areproductivecell11 betahydroxylaseAccountsfor 5-8%of CAHcasesDHTActive formoftestosteroneMRKHCanpresentsimilar toAISMeiosisProcess bywhichoogoniabecomeoocytes GranulosacellsA single layerof these cellsis found inprimordialfolliclesAdrenalcrisisWhathappens toCAH babyafter deliveryOogoniaThesediploid germcells developinto oocytesACTHIncreasedproduction inpituitary ofCAH babiesMesonephrosDescribedby CasparWolff in1759VirilizedfemalePreferred overfemalepseudo-hermaphroditeby DrGDexamethasoneSteroidtreatment hatedby pregnantwomen at riskfor baby withCAHHOXGenesControl expressionof growth factorsthat induce thestraight wolffianduct to elongateand coil OutercortexConsists ofovarianfollicles andstroma inbetween themClassicCAHCan haveboth salt-wasting andsimplevirilizing formsThecaluteincysts10-20% inwomen withgestationaltrophoblasticdisease RenalsystemAnomalies inthis systemoften found inpatients withmulleriananomaliesPGDCan be usedwith IVF toscreen forCAHLuteomaHyperplasticmassof luteinized cells1/3 associatedwith maternalhirsutismor virilization herniauterineinguinalesyndromeProbably thediagnosis ofthe Pope inConclaveUndervirilizedmalePreferred overmale pseudo-hermaphroditeby DrGHermaphroditusIn Greekmythologywas a childof Aphroditeand Hermes.IncompleteAISphenotype ispredominantlyundervirilizedmale withgreat range SertolicellsCells thatnourishmake germcells intubulesTruehermaphroditeIndividualwith bothovarian andtesticulartissueCortisolSteroid that isproduced from11-deoxycortisolby 11hydroxylase5alphareductaseEnzymethatconverts Tto DHT17hydroxylasedeficiencyrare causeof CAH with~ 100 casesreported 6-7millionNumber ofoogonia at20 weeksgestationSRYRegion of Ychromosomethat leads tomaledevelopmentalpathwayPrimordialfolliclesThe structurethat formswhen anoogoniummatures.InnermedullaryregionContainsovarianblood vessels,lymphaticvessels,and nerves.HyperpigmentationFrequentlyseem incasesof high levelsof ACTHPrincetonDrG almamater andwhere authorof Middlesexwas on faculty21hydroxylaseDeficiency ismostcommoncause ofCAHSimplevirilizingNon-lethalform ofclassicCAHReteovariiVestigialtubules andLeydig cells inhilarregion of ovary PlacentaProtectsCAH fetusprior todeliveryYupicEskimoHighestcarrierfrequencyof CAH1/3Odds thatphenotypicsisters ofaffectedindividualare XYGermline stemcellsMice seemto havethese butwe may notY containingIntrabdominalgonadNeedsto beremovedTestosterone19 carbonsteroidconvertedinto DHTMiddlesexNovel byJeffreyEuginidesCompoundheterozygoteNon-classicforms of 21Hydroxylasedeficiency areusually thisgenetic mixturePseudogeneCommonmutationin classicCAHhCGStimTestcan distinguishbetween 5αreductasedeficiency, defectsin testosteronesynthesis andincomplete AIS 20weeksgestationAge withmaximumnumber offemale germcellsWolffianductsMale ductsnamed afterfamousGermanembryologistand anatomist1/6Odds offemaleoffspring ofnormal sisterwill be 46 XYAlfredJostExperimentswith rabbitsexplained roleof local T inmaledevelopmentSaltwastingSpecific formof classicCAH leadingto neonataldeathSomaticcellsIn the absenceof ovarian germcells theseovarian cellsfail to developTGF-betasuperfamilyAMH is amember ofthis super-family6metersLength ofhumanepididymisVirilizationLoss of femalebody contours,deepeningvoiceclitoromegalyetc17 hydroxyprogesteroneLab testused toevaluatefor CAHLeydigcellsAndrogenproducingcells intestesCompleteAISfirst describedat Yale whereMorris coinedthe term“testicularfeminization” Para-mesonephrousDescribed byJohannesMuller in1830AMHTGF-beta familymember thatcausesregressionof mullerianductNomogramUsed tocomparebasal andstim levels of17-OHPACTHStimtestUsed toscreenfor CAHMetanephrousDevelopsintothe renalsystemMullerianductsNamed afterfamousembryologistthese ductsdevelop intofemale reproductivesystem 1-2%enzymeactivityPatients withsimple virilizingmost often havepoint mutationswith ___enzyme activity GermcellsA cell thatdevelopsinto areproductivecell11 betahydroxylaseAccountsfor 5-8%of CAHcasesDHTActive formoftestosteroneMRKHCanpresentsimilar toAISMeiosisProcess bywhichoogoniabecomeoocytes GranulosacellsA single layerof these cellsis found inprimordialfolliclesAdrenalcrisisWhathappens toCAH babyafter delivery

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.


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