Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21-OHD) in adult males: Clinical presentation, hormone function and the detection of adrenal and testicular adrenal rest tumors (TARTs)

Endocrinologia, Diabetes y Nutricion - Tập 68 - Trang 227-235 - 2021
Patricia San Martín1, María Laura Eugenio Russmann1, Gabriela Mendeluk2, María Fabiana Fierro1, Roxana Marino3, Ester Pardes1
1Department of Endocrinology, Hospital JM Ramos Mejía, Urquiza 609, Zip Code 1221, Buenos Aires, Argentina
2Unit of Clinical Cytology, Hospital JM Ramos Mejía, Urquiza 609, Zip Code 1221, Buenos Aires, Argentina
3Department of Endocrinology, Hospital de Pediatría JP Garrahan, Pichincha 1890, Zip Code 1245, Buenos Aires, Argentina

Tài liệu tham khảo

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