A case of a fetus diagnosed prenatally with classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is discussed, highlighting the importance of early diagnosis and care.
The interdisciplinary approach, involving perinatology, endocrinology, genetic counseling, psychology, and urology, allowed for better management and support for the family.
Fetal MRI combined with ultrasound revealed significant brain anomalies, indicating a need for further investigation into neurological issues associated with CAH from a prenatal perspective.