Table shows that Turner syndrome occurs when an individualinherits one X chromosome but lacks a second sex chromosome.Can Turner syndrome be due to nondisjunction duringoogenesis, spermatogenesis, or both? If a phenotypically normalcouple has a color-blind child (due to a recessive X-linkedallele) with Turner syndrome, did nondisjunction occur duringoogenesis or spermatogenesis in this child’s parents? Explainyour answer. TABLE 8.1Aneuplold Conditions in HumansConditionFrequency SyndromeCharacteristicsAutosomalTrisomy 131/15,000PatauMental and physical deficlen-cles, wide varlety of defectsIn organs, large trilangularnose, early deathMental and physicaldeficlencles, faclal abnor-malitles, extreme muscleTrisomy 181/6000Edwardtone, early deathTrisomy 211/800DownMental deficlencles, abnormalpattern of palm creases,slanted eyes, flattened face,short statureSex Chromosomal1/1000KlinefelterSexual Immaturity (no sperm[males), breast swellingXXYXYY1/1000JacobsTall and thin (males)XXX1/1500Triple XTall and thin, menstrualIrregularity (females)хо1/5000TurnerShort stature, webbedneck, sexually undeveloped(females)

Name: Table shows that Turner syndrome occurs when an individualinherits one
Uploaded: 2024-03-20T06:43:04.000Z
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Description: Table shows that Turner syndrome occurs when an individualinherits one X chromosome but lacks a second sex chromosome.Can Turner syndrome be due to nondisjunction duringoogenesis, spermatogenesis, or both? If a phenotypically normalcouple has a color