17α-hydroxylase/17,20-lyase deficiency

PrepTutorEJDIC

1. 〈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

UpToDate Contents

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

• 1. 先天性副腎過形成の稀な原因 uncommon causes of congenital adrenal hyperplasia
• 2. 小児における原発性副腎不全の原因および臨床症状 causes and clinical manifestations of primary adrenal insufficiency in children
• 3. 副腎ステロイド生合成 adrenal steroid biosynthesis
• 4. 21－ヒドロキシラーゼ欠損症による古典的先天性副腎皮質過形成の遺伝学および
  臨床症状 genetics and clinical presentation of classic congenital adrenal hyperplasia due to 21 hydroxylase deficiency
• 5. 副腎アンドロゲンの測定 measurement of adrenal androgens

Japanese Journal

• Abnormal steroidogenesis in three patients with Antley-Bixler syndrome : Apparent decreased activity of 17α-hydroxylase, 17,20-lyase and 21-hydroxylase

• ADACHI MASANORI,ASAKURA YUMI,TACHIBANA KATSUHIKO,SHACKLETON CEDRIC
• Pediatrics international : official journal of the Japan Pediatric Society 46(5), 583-589, 2004-10-01
• NAID 10016544012

Related Links

• Congenital adrenal hyperplasia due to 17 alpha-hydroxylase ...

A very small number of people have reportedly had an abnormal allele that resulted primarily in a reduction of 17,20-lyase activity, rather than both the hydroxylase and lyase activities as ...

---

★リンクテーブル★

リンク元	「17α-水酸化酵素/17,20-リアーゼ欠損症」
関連記事	「deficiency」

「17α-水酸化酵素/17,20-リアーゼ欠損症」

　　[★]

英

17α-hydroxylase/17,20-lyase deficiency

関

先天性副腎過形成

「deficiency」

　　[★]

• n.

• 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