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Review Question - QID 213638

Adrenogenital Syndrome (Congenital Adrenal Hyperplasia) 11β-Hydroxylase Deficiency Presentation QID: 213638 (M1.OMB.19.1)
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QID 213638 (Type "213638" in App Search)
A 7-year-old girl is brought to a pediatrician to establish care after her parents moved to a new state. She was born at full term and has no significant past medical history. On physical exam, her blood pressure is 151/91 mmHg and her pulse is 91/min. She is also found to have early development of axillary and pubic hair. Upon further questioning, her parents say that her genitalia were somewhat ambiguous at birth and physical exam reveals clitoral enlargement and labioscrotal fusion. Which of the following enzymes is most likely defective in this patient?
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