Template:BGDB Sexual Differentiation - Abnormalities Interactive: Difference between revisions
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<quiz display=simple> | <quiz display=simple> | ||
{ | {In a genetic male (44 x XY) who lacks androgen receptors, each of the following will be increased except: | ||
|type="()"} | |type="()"} | ||
- | - estradiol | ||
- | || Incorrect! | ||
- FSH | |||
|| | || Incorrect! | ||
- LH | |||
- | || Incorrect! | ||
+ progesterone | |||
|| Correct! | |||
- testosterone | |||
|| Incorrect! | |||
{The best option below for a child born with ambiguous external genitalia could be: | |||
|type="()"} | |||
- 46,XX DSD a female pseudohermaphrodite | |||
|| Correct! But not the best answer option, that is any of the above. '''46,XX DSD''' used to be called a "female pseudohermaphrodite", please use the modern terminology for this {{DSD}} | |||
- 46,XY DSD a male pseudohermaphrodite | |||
|| Correct! But not the best answer option, that is any of the above. '''46,XY DSD''' used to be called a "male pseudohermaphrodite", please use the modern terminology for this {{DSD}} | |||
- Ovotesticular DSD | |||
|| Correct! But not the best answer option, that is any of the above. '''Ovotesticular DSD''' used to be called a "true hermaphrodite", please use the modern terminology for this {{DSD}}. | |||
- someone with Klinefelter’s syndrome | |||
|| Correct! {{Klinefelter’s syndrome}} is a possibility, but not the best answer option, that would be any of the above. | |||
+ any of the above | |||
|| Correct! | |||
{In monosomy XO (Turner’s syndrome): | |||
|type="()"} | |||
- the children start normal male development | |||
|| Incorrect! In monosomy XO ({{Turner’s syndrome}}) the number of germ cells in the gonads starts decreasing after {{puberty}}. | |||
+ the number of germ cells in the gonads starts decreasing after puberty | |||
|| Correct! In monosomy XO ({{Turner’s syndrome}}) the number of germ cells in the gonads starts decreasing after {{puberty}}. | |||
- the children grow disproportionately tall | |||
|| Incorrect! In monosomy XO ({{Turner’s syndrome}}) the number of germ cells in the gonads starts decreasing after {{puberty}}. | |||
- an active gene on a dormant X chromosome may account for the clinical manifestations | |||
|| Incorrect! In monosomy XO ({{Turner’s syndrome}}) the number of germ cells in the gonads starts decreasing after {{puberty}}. | |||
- all of the above might occur | |||
|| Incorrect! In monosomy XO ({{Turner’s syndrome}}) the number of germ cells in the gonads starts decreasing after {{puberty}}. | |||
{If 46,XY DSD is due to androgen receptor disorders, then: | |||
|type="()"} | |||
- the testes are normal for the most part | |||
|| Correct! But not the best answer, all of the above options can be correct. | |||
- the testosterone and DHT levels are normal | |||
|| Correct! But not the best answer, all of the above options can be correct. | |||
- MDIF is secreted by the Sertoli cells | |||
|| Correct! But not the best answer, all of the above options can be correct. | |||
- the fetus will have female external genitalia without a female genital tract | |||
|| Correct! But not the best answer, all of the above options can be correct. | |||
+ all of the above is correct | |||
|| Correct! All of the above options can be correct. | |||
{Failure of formation and migration of the primordial germ cells results in: | |||
|type="()"} | |||
- Turner’s syndrome | |||
|| Incorrect! Failure of formation and migration of the primordial germ cells results in gonadal agenesis. | |||
- Klinefelter’s syndrome | |||
|| Incorrect! Failure of formation and migration of the primordial germ cells results in gonadal agenesis. | |||
- 46,XX DSD | |||
|| Incorrect! Failure of formation and migration of the primordial germ cells results in gonadal agenesis. | |||
+ gonadal agenesis | |||
|| Correct! Failure of formation and migration of the primordial germ cells results in gonadal agenesis. | |||
- none of the above | |||
|| Incorrect! Failure of formation and migration of the primordial germ cells results in gonadal agenesis. | |||
{Failure of the urethral folds to fuse prenatally would be expected to result in: | |||
|type="()"} | |||
- epispadias | |||
|| Incorrect! Failure of the urethral folds to fuse prenatally would be expected to result in {{hypospadias}} | |||
- exstrophy of urinary bladder | |||
|| Incorrect! Failure of the urethral folds to fuse prenatally would be expected to result in {{hypospadias}} | |||
- horseshoe kidney | |||
|| Incorrect! Failure of the urethral folds to fuse prenatally would be expected to result in {{hypospadias}} | |||
+ hypospadias | |||
|| Correct! Failure of the urethral folds to fuse prenatally would be expected to result in {{hypospadias}} | |||
- multiple ureters | |||
|| Incorrect! Failure of the urethral folds to fuse prenatally would be expected to result in {{hypospadias}} | |||
</quiz> | </quiz> | ||
Latest revision as of 23:28, 2 Haziran 2019
Abnormalities Interactive Component
| Attempt the Quiz - Abnormalities | ||
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Here are a few simple Quiz questions that relate to Abnormalities of genital development from the lecture and practical.
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