Otto syndrome

オットー症候群

WordNet

1. a pattern of symptoms indicative of some disease
2. a complex of concurrent things; "every word has a syndrome of meanings"

PrepTutorEJDIC

1. (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

UpToDate Contents

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• 1. マルファン症候群および関連疾患のマネージメントmanagement of marfan syndrome and related disorders [show details]
  …patient specific considerations. The UpToDate editorial staff would like to thank Dr. Catherine M. Otto for her contributions as Section Editor to previous versions of this topic review.…
• 2. ターナー症候群の臨床症状と診断clinical manifestations and diagnosis of turner syndrome [show details]
  …and cubitus valgus in a paper published in 1938 by Henri Turner, an Oklahoma physician . However, Otto Ulrich had already described an eight-year-old girl with a similar phenotype several years earlier…
• 3. マルファン症候群および関連疾患の遺伝学、臨床的特徴、および診断genetics clinical features and diagnosis of marfan syndrome and related disorders [show details]
  …second-degree relatives is reasonable. The UpToDate editorial staff would like to thank Dr. Catherine M. Otto for her contributions as Section Editor to previous versions of this topic review.…
• 4. 人工弁置換後の僧帽弁閉鎖不全症や大動脈弁閉鎖不全症の臨床症状および診断clinical manifestations and diagnosis of surgical aortic and mitral prosthetic valve regurgitation [show details]
  …staff would like to thank Dr. William H. Gaasch for his past contributions as author and Dr. Catherine Otto for her past contributions as section editor to prior versions of this topic review.…
• 5. 頚静脈波の検討examination of the jugular venous pulse [show details]
  …UpToDate editorial staff would like to thank Bernard Gersh, MB, ChB, DPhil, FRCP, MACC, Catherine M. Otto, MD, and the late Kanu Chatterjee, MB, FRCP, FCCP, FACC, MACP, for their contributions to prior versions…

English Journal

• An uncommon case of arthrogryposis, renal dysfunction, and cholestasis (ARC) syndrome and review of the renal involvement: Answers.

• Duong MD, Rose CM, Reidy KJ, Del Rio M.
• Pediatric nephrology (Berlin, Germany). 2020 Feb;35(2)249-251.
• PMID 31463586

• An uncommon case of arthrogryposis, renal dysfunction, and cholestasis (ARC) syndrome and review of the renal involvement: Questions.

• Duong MD, Rose CM, Reidy KJ, Del Rio M.
• Pediatric nephrology (Berlin, Germany). 2020 Feb;35(2)247-248.
• Arthrogryposis, renal dysfunction, and cholestasis syndrome is a rare autosomal recessive disorder caused by mutations in the VPS33B and VIPAR genes. Most cases are fatal within the first year of life. Here we describe one of the two oldest patients with arthrogryposis, renal dysfunction, and choles
• PMID 31463585

• 7T magnetic resonance neurography-ultrasound fusion for peripheral nerve imaging.

• Schreiber S, Schreiber F, Peter A, Isler E, Dörner M, Heinze HJ, Petri S, Tempelmann C, Nestor PJ, Grimm A, Vielhaber S.
• Muscle & nerve. 2020 Jan;().
• We present one patient with an initial diagnosis of Guillain-Barré syndrome (GBS) and one with Charcot-Marie-Tooth disease (CMT) type 1A. Both patients underwent ankle tibial nerve fusion-imaging of high-resolution ultrasound (HRUS) with 7T magnetic resonance neurography (MRN). In GBS, the nerve wa
• PMID 31899543

Japanese Journal

• Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmoduline

• Nat Genet. 37, 282-288, 2005
• NAID 80017161830

• 糖尿病による足の病変及びフットケアー ・ コンセプトを用いた保存療法

• 日本義肢装具学会誌 = Bulletin of the Japanese Society of Prosthetic and Orthotic Education, Research and Development 18(3), 214-220, 2002-07-01
• NAID 10010052439

• Surgical treatment of West syndrome

• Brain & development 23(7), 668-676, 2001-10-01
• NAID 50001008196

Related Links

• Otto syndrome | definition of Otto syndrome by Medical dictionary

limitation of range of joint motion and contractures present at birth, usually involving multiple joints; a syndrome probably of diverse etiology that may result from changes in spinal cord, muscle, or connective tissue. Several forms ...

• Otto syndrome - RightDiagnosis.com

Otto syndrome symptoms, causes, diagnosis, and treatment information for Otto syndrome (Arthrogryposis) with alternative diagnoses, full-text book chapters, misdiagnosis, research treatments, prevention, and prognosis.

• GRJ ジュベール症候群

Varadi-Papp syndrome（OFD VI型）は、小脳虫部の低形成、口腔小帯、舌の過誤腫、正中線の口唇列が挙げられ、同様に異なる特徴のY字型中手骨を伴う中央列多指症が挙げられる [Munke et al 1990]。腎臓と心臓の合併症も報告さ

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★リンクテーブル★

リンク元	「先天性多発性関節拘縮症」
関連記事	「syndrome」

「先天性多発性関節拘縮症」

　　[★]

英

congenital multiple arthrogryposis

ラ

arthrogryposis multiplex congenita AMC

同

オットー症候群 Otto syndrome

関

先天性筋形成不全症

[show details]

先天性多発関節彎曲 : 19 件
先天性多発関節彎曲症 : 18 件
先天性多発性関節拘縮 : 約 89 件
先天性多発性関節拘縮症 : 約 89 件

「syndrome」

　　[★]

• n.

• 症候群