11β-水酸化酵素欠損症
PrepTutorEJDIC
- 〈U〉〈C〉(…の)(量・額などの)不足,欠乏《+『of』(『in』)+『名』》 / 〈C〉不足分,不足量,不足額 / 〈C〉(精神・肉体などの)欠陥
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Japanese Journal
- Leydig Cell Tumor and Malignant Lymphoma in a Patient with Nonclassical 21-Hydroxylase Deficiency
- Inaba Hidefumi,Suzuki Satoru,Shigematsu Satoshi,Shinomiya Ken,Ohfusa Hirokazu,Shimojo Yasuyo,Uehara Takeshi,Hashizume Kiyoshi
- Internal Medicine 48(8), 601-605, 2009
- … Based on the laboratory results, he was diagnosed as congenital adrenal hyperplasia (CAH) due to nonclassical 21-hydroxylase deficiency (21-OHD). … On immunohistochemistry analysis using the antibody against adrenal-specific 11β-hydroxylase antibody, the LCT showed both properties as a testicular cell and as an adrenal cell. …
- NAID 130000108034
- 4歳からフォローアップされ, 新しいCYP11B1遺伝子変異が同定された先天性副腎皮質過形成 (11β-hydroxylase 欠損症) の37歳男子例
- 小川 正道,矢沢 武,森 理,上條 隆司,月舘 幸一,立松 寿,冨田 博,勝又 規行
- ホルモンと臨牀 55(2), 173-179, 2007-02-01
- NAID 10018586539
Related Links
- 11β-Hydroxylase enzymes CYP11B1 and CYP11B2 catalyze the final biosynthetic steps in the production of cortisol and aldosterone. Deficiency of CYP11B1 is the s ... Classical CAH is the term used when the enzymatic ...
- 11β hy·drox·y·lase de·fi·cien·cy (hi drokґsə lās) an autosomal recessive disorder of steroidogenesis caused by a mutation in the CYP11B1 gene (locus: 8q21), which encodes steroid 11β monooxygenase; the ... 11β-hydroxylase ...
Related Pictures
★リンクテーブル★
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- 英
- 11β-hydroxylase deficiency 11beta-hydroxylase deficiency
- 同
- 11β-ヒドロキシラーゼ欠損症 11βヒドロキシラーゼ欠損症、11β水酸化酵素欠損症
- 関
- 11β-水酸化酵素
[show details]
[★]
- 不足、欠乏、欠失、欠如、欠損、不十分。栄養不足、栄養素欠乏、欠乏症。(遺伝子)(染色体内の)遺伝子欠失
- 欠けているもの、不足している物。不足分。不完全なもの、欠点のあるもの
- 関
- absence, agenesis, dearth, defect, defective, deficient, deficit, delete, deletion, deletional, depletion, deprivation, deprive, lack, miss, missing, morphological defect, paucity, scarce, scarcity, starve