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Classical 11β-Hydroxylase Deficiency Caused by a Novel Homozygous Mutation: A Case Study and Literature Review

Mohammad N Alsanea1, Abdulmoein Al-Agha2, Mohamed Abdelmaksoud Shazly2

  • 1Internal Medicine, King Abdulaziz University Faculty of Medicine, Jeddah, SAU.

Cureus
|February 2, 2022
PubMed

Keywords:
adrenalatypical genitaliacongenitalhyperplasiahypertension

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