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Autor:
R. D. Gaag, Hemmo A. Drexhage, C. D. Kooyman, Louis Kater, F. J. H. Gmelig Meyling, H. J. Schuurman, D. Jolink, R. J. M. Croughs, F. Teding Van Berkhout
Publikováno v:
Clinical endocrinology. 24(3)
SUMMARY Two sisters aged 13 and 19 years suffering from familial Cushing's syndrome due to nodular adrenocortical dysplasia are described. Pituitary adrenocortical function tests indicated the presence of adrenal autonomy. Adrenal scintigraphy showed