オピッツ症候群
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- 1. ディジョージ(22q11.2欠失)症候群:臨床的特徴および診断digeorge 22q11 2 deletion syndrome clinical features and diagnosis [show details]
…association patients. The Opitz G/BBB syndrome is characterized by ocular hypertelorism, asymmetry of the skull, hypospadias, and laryngoesophageal defects . These features distinguish Opitz G/BBB from DGS. The …
- 2. ダウン症の母体血清スクリーニングに関する臨床検査の問題laboratory issues related to maternal serum screening for down syndrome [show details]
…predictable. These cases may be identified by second-trimester trisomy 18 screening protocols. Smith-Lemli-Opitz syndrome (SLOS) is an autosomal recessive defect in a cholesterol biosynthetic enzyme, C7-reductase…
- 3. 光線過敏症(光線皮膚症):臨床症状、診断、および治療photosensitivity disorders photodermatoses clinical manifestations diagnosis and treatment [show details]
…hepatoerythropoietic porphyria. Diagnosis and treatment of the porphyrias are discussed separately. Smith-Lemli-Opitz syndrome is a rare, congenital, multiple anomaly syndrome caused by an inborn error of cholesterol …
- 4. 性分化の差の原因causes of differences of sex development [show details]
…17-beta-hydroxysteroid dehydrogenase (17-beta-HSD) deficiency; 5-alpha reductase deficiency; Smith-Lemli-Opitz syndrome; These and some even rarer causes of DSDs are described below and outlined in the tables…
- 5. 症候群をきたす免疫不全症syndromic immunodeficiencies [show details]
…velocardiofacial syndrome (VCFS), and (less commonly) Opitz G/BBB (oculogenitolaryngeal) syndrome. DiGeorge syndrome and VCFS are reviewed in more detail separately. The Opitz G/BBB syndrome is characterized by ocular …
★リンクテーブル★
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- 英
- Opitz syndrome
- 同
- オピッツ・フリアス症候群 Opitz-Frias syndrome、両眼開離尿道下裂症 telecanthus hypospadias、Opitz oculo-genito-laryngeal syndrome
- Opitz syndrome , Opitz-Frias syndrome a familial syndrome consisting of hypertelorism and hernias, and in males also characterized by hypospadias, cryptorchidism, and bifid scrotum. Cardiac, laryngotracheal, pulmonary, anal, and renal abnormalities may also be present.
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オピッツ・フリアス症候群
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- 英
- syndrome, symptom-complex
- 同
- 症状群
- 関
- [[]]
- 成因や病理学的所見からではなく、複数の症候の組み合わせによって診断される診断名あるいは疾患。
内分泌
先天的代謝異常
高プロラクチン血症
- 分娩後の視床下部障害によるプロラクチン分泌抑制因子の分泌抑制のため、高プロラクチン血症を呈する。
- 分娩に関係なくプロラクチン分泌抑制因子の分泌抑制をきたし、高プロラクチン血症を呈する。
性腺機能低下
- 嗅覚の低下・脱出、低ゴナドトロピン性性腺機能低下症
- 肥満、網膜色素変性症、知能低下、低ゴナドトロピン性性器発育不全、多指症、低身長
性早熟
- 思春期早発症、多発性線維性骨異形成症、皮膚色素沈着
- 女性型の肥満、性器の発育障害の2主徴を示し、視床下部に器質的障害をもつ疾患群。
脳神経外科・神経内科
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- 英
- group
- 関
- グループ、集団、分類、群れ、基、グループ化
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- 英
- symptom and sign
- 関
- 症状, 徴候 兆候