Brachmann-de Lange syndrome

ブラックマンドランゲ症候群

WordNet

1. a legal document signed and sealed and delivered to effect a transfer of property and to show the legal right to possess it; "he signed the deed"; "he kept the title to his car in the glove compartment" (同)deed of conveyance, title
2. a pattern of symptoms indicative of some disease
3. a complex of concurrent things; "every word has a syndrome of meanings"
4. go `ding dong, like a bell (同)dong, dingdong
5. a ringing sound
6. United States photographer remembered for her portraits of rural workers during the Depression (1895-1965) (同)Dorothea Lange

PrepTutorEJDIC

1. 『行為』,行動 / (正式の)捺印証書,権利書 / …'を'証書を作製して譲渡する
2. (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
3. 〈鐘など〉‘を'ガンガン鳴らす / 〈鐘などが〉ガンガン鳴る / (鐘の)ガンガン鳴る音
4. (おもに人称代名詞・固有名詞(人名),thereの後で)had, wouldの短縮形 / (疑問文でwhere,what,whenの後で)didの短縮形;Where'd he go?=Where did he go?

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• 1. 先天性奇形に対するアプローチ approach to congenital malformations
• 2. 先天性横隔膜ヘルニア：出生前診断およびマネージメント congenital diaphragmatic hernia prenatal diagnosis and management
• 3. 萎縮性毛孔性角化症 keratosis pilaris atrophicans
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• 5. 小児における停留精巣：臨床的特徴および評価 undescended testes cryptorchidism in children clinical features and evaluation

English Journal

• An experimental study of executive function and social impairment in Cornelia de Lange syndrome.

• Nelson L1,2, Crawford H3,4, Reid D1, Moss J1,5, Oliver C1.
• Journal of neurodevelopmental disorders.J Neurodev Disord.2017 Sep 11;9(1):33. doi: 10.1186/s11689-017-9213-x.
• PMID 28889797

• Connected Gene Communities Underlie Transcriptional Changes in Cornelia de Lange Syndrome.

• Boudaoud I1,2, Fournier É1,2, Baguette A1,2, Vallée M1, Lamaze FC1,2, Droit A1,3, Bilodeau S4,2,5.
• Genetics.Genetics.2017 Sep;207(1):139-151. doi: 10.1534/genetics.117.202291. Epub 2017 Jul 5.
• PMID 28679547

• Cornelia de lange syndrome with thyroid agenesis of an indonesian patient.

• Maskoen AM1, Laksono B1, Hajjah R2, Zada A3, Suciati LP4, Fauziah PN4, Nataprawira HM2.
• Cellular and molecular biology (Noisy-le-Grand, France).Cell Mol Biol (Noisy-le-grand).2017 Aug 30;63(8):93-94. doi: 10.14715/cmb/2017.63.8.19.
• PMID 28886330

Japanese Journal

• Spinal anesthesia in a child with Brachmann-de Lange (Cornelia de Lange) syndrome

• Journal of anesthesia 24(6), 942-944, 2010-12-20
• NAID 10027741697

• Brachmann-de Lange syndrome with congenital diaphragmatic hernia and NIPBL gene mutation

• Congenital anomalies 50(2), 129-132, 2010-06-01
• NAID 10029577887

• Cornelia de Lange syndrome (Brachmann-de Lange syndrome)

• 症候群事典 78(増刊), 79, 2006
• NAID 50006064283

Related Links

• Cornelia de Lange Syndrome - GeneReviews® - NCBI Bookshelf

Classic Cornelia de Lange syndrome (CdLS) is characterized by distinctive facial features, growth retardation (prenatal onset; <5th centile throughout life), hirsutism, and upper limb reduction defects that range from subtle ...

• GRJ コルネリア デ ランゲ症候群

GRJ top ＞ 遺伝子疾患情報リスト コルネリア デ ランゲ症候群 (Cornelia de Lange Syndrome) [BDLS, Brachmann-de Lange Syndrome, CdLS, de Lange Syndrome. Includes: NIPBL-Related Cornelia de Lange Syndrome, SMC1A ...

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★リンクテーブル★

リンク元	「ブラックマンドランゲ症候群」
関連記事	「DE」「syndrome」

「ブラックマンドランゲ症候群」

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英

Brachmann-de Lange syndrome

同

Brachmann-de Lange症候群

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　　[★] 線量当量 dose equivalent 　

「syndrome」

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• n.

• 症候群