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This case report describes a 29-year-old male patient presenting with azoospermia and no significant medical or family history. Laboratory tests found normal testosterone levels with low-normal LH and FSH levels, ruling out hypogonadotropic hypogonadism. A testicular biopsy was compatible with congenital adrenal hyperplasia (CAH). The patient was found to have extremely high levels of 17-hydroxyprogesterone, confirming 21-hydroxylase deficiency CAH. Treatment with glucocorticoids normalized testicular devel

Author

Engels Yeltsin Ponce Gonzales

Language

EN