You are reviewing a 9-year-old female child in the paediatric genetic disorders’ clinic, who has a confirmed diagnosis of congenital adrenal hyperplasia.
You are reviewing a 9-year-old female child in the paediatric genetic disorders’ clinic, who has a confirmed diagnosis of congenital adrenal hyperplasia. They are short in stature and have reached menarche already. Which of the following signs would also be characteristic of congenital adrenal hyperplasia due to 21-hydroxylase mutation?
Select the SINGLE most appropriate option from the list below. Select ONE option only.
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