21-Hydroxylase Deficiency Presenting as Massive Bilateral Adrenal Masses in the Seventh Decade of Life

A 72-year-old woman was found to have massive bilateral adrenal masses on computed tomography and was diagnosed with 21-hydroxylase deficiency (21-OHD) based on endocrinological findings. Physical examination revealed no abnormalities except markedly short stature. She was diagnosed with 21-OHD beca...

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Veröffentlicht in:	Endocrine Journal 1999, Vol.46(6), pp.817-823
Hauptverfasser:	ABO, KATSUMI, SUMINO, KIMIAKI, NISHIO, HISAHIDE, HOZUMI, TOSHIKI, ISHIDA, YOSHIHIKO, FUJIEDA, KENJI, TAJIMA, TOSHIHIRO, KAZUMI, TSUTOMU
Format:	Artikel
Sprache:	eng
Schlagworte:	21-Hydroxylase deficiency Adrenal Cortex - diagnostic imaging Adrenal Cortex - pathology Adrenal Hyperplasia, Congenital - diagnostic imaging Adrenal Hyperplasia, Congenital - etiology Adrenal Hyperplasia, Congenital - genetics Adrenal Hyperplasia, Congenital - pathology Aged Bilateral adrenal masses CYP21 gene Fatal Outcome Female Gene Deletion Humans Mutation - genetics Steroid 21-Hydroxylase - genetics Tomography, X-Ray Computed
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