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Kaplan Qbank USMLE



Author7 Posts
  #1

A 4 year old 46,XY male presents with hyperpigmentation, clitoromegaly, no labial fusion and blind vaginal pouch. Further examination reveals hypoplastic male genital ducts but no Mullerian development. CT scan shows,large,lipid-laden adrenals causing downward displacement of the kidneys. Lab findings show low levels of all C21, C17, C18 steroids in the plasma and urine, and absent response to ACTH and hCG stimulation.What deficiency does the patient have

a) 21-alpha hydroxylase

b) Aromatase

c) 11 beta hydroxylase
d) Steroidgenic acute regulatory protein
e) 17-alpha hydroxylase



  #2

D lipoid congenital adrenal hyperplasia.

  #3

D

  #4

this one i dont know u will have to explain it to me man am i groggy

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FORUM RULES-- Those who believe in telekinesis, raise my hand. I get enough exercise just by pushing my luck --P4U World.." The pure and simple truth is rarely pure and never simple."

  #5

Only after doing research on Steroidgenic acute regulatory protein , I'm answering D.

Is it a lipoid congenital adrenal hyperplasia ?




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Prioritize & simplify.

  #6

ACTH stimulation understood,whats hCG stimulation?

  #7

D







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