| Item type |
デフォルトアイテムタイプ_（フル）(1) |
| 公開日 |
2023-03-18 |
| タイトル |
|
|
タイトル |
A Case of Cogenital Adrenal Hyperplasia with Concomitant Abnormalities of Steroid 21- and 11β-hydroxylase Activities |
|
言語 |
en |
| 作成者 |
Egusa, Genshi
Mori, Hiroshi
Yamane, Kiminori
Okamura, Midori
Oda, Kiyoshi
Ishida, Sakurako
Kado, Seijiro
Hara, Hitoshi
Yamakido, Michio
|
| アクセス権 |
|
|
アクセス権 |
open access |
|
アクセス権URI |
http://purl.org/coar/access_right/c_abf2 |
| 主題 |
|
|
主題Scheme |
Other |
|
主題 |
Congenital adrenal hyperplasia |
| 主題 |
|
|
主題Scheme |
Other |
|
主題 |
21-hydroxylase |
| 主題 |
|
|
主題Scheme |
Other |
|
主題 |
11β-hydroxylase |
| 主題 |
|
|
主題Scheme |
NDC |
|
主題 |
490 |
| 内容記述 |
|
|
内容記述 |
Abnormalities in the steroid 21-hydroxylase and 11β-hydroxylase activities were suspeted in a 25-year-old female with congenital adrenal hyperplasia (CAH). The patient showed signs of masculinization such as hirsutism, amenorrhea, and enlarged clitoris, but the blood pressure was normal. Adrenocorticotropic was increased to 200 pg/ml. Plasma levels of deoxycorticosterone and 11-deoxyortisol as well as progesterone and 17-hydroxyprogesterone were elevated. Plasma cortisol level was normal at 5.8 μg/dl. CT scan revealed enlargement of the bilataral adrenal glands. This case suggests that enzyme abnormalities in CAH are more diverse than have been generally considered. |
|
言語 |
en |
| 出版者 |
|
|
出版者 |
Hiroshima University Medical Press |
| 言語 |
|
|
言語 |
eng |
| 資源タイプ |
|
|
資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
|
資源タイプ |
departmental bulletin paper |
| 出版タイプ |
|
|
出版タイプ |
VoR |
|
出版タイプResource |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| 関連情報 |
|
|
|
識別子タイプ |
PMID |
|
|
関連識別子 |
2086566 |
| 収録物識別子 |
|
|
収録物識別子タイプ |
ISSN |
|
収録物識別子 |
0018-2052 |
| 収録物識別子 |
|
|
収録物識別子タイプ |
NCID |
|
収録物識別子 |
AA00664312 |
| 開始ページ |
|
|
開始ページ |
145 |
| 書誌情報 |
Hiroshima Journal of Medical Sciences
Hiroshima Journal of Medical Sciences
巻 39,
号 4,
p. 145-147,
発行日 1990-12
|
| 旧ID |
38092 |
HiroshimaJMedSci_39_145.pdf (293.3 KB)
