ヘクト・ビールズ症候群
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
- United States writer of stories and plays (1894-1946) (同)Ben Hecht
PrepTutorEJDIC
- (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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English Journal
- Successful difficult airway management in a child with Hecht-Beals syndrome.
- Kumar A1, Chandran R, Khanna P, Bhalla AP.
- Indian journal of anaesthesia.Indian J Anaesth.2012 Nov;56(6):591-2. doi: 10.4103/0019-5049.104591.
- PMID 23325953
- Trismus-pseudocamptodactyly syndrome (Hecht-Beals' syndrome): case report and literature review.
- Carlos R1, Contreras E, Cabrera J.
- Oral diseases.Oral Dis.2005 May;11(3):186-9.
- The trismus-pseudocamptodactyly syndrome (TPS) is a rare condition inherited as an autosomal dominant trait with variable expressivity. Clinically the syndrome is characterized by decreased ability to open the mouth and curvature of the fingers at the level of interphalangic joints while attempting
- PMID 15888111
- Anaesthetic management of two paediatric patients with Hecht-Beals syndrome.
- Nagata O1, Tateoka A, Shiro R, Kimizuka M, Hanaoka K.
- Paediatric anaesthesia.Paediatr Anaesth.1999;9(5):444-7.
- We undertook the anaesthetic management of two children with Hecht-Beals syndrome for orthopaedic surgery under general anaesthesia. Both patients had arachnodactyly, kyphoscoliosis, and multiple congenital joint contractures, but limited mandible excursion was not obvious preoperatively in either,
- PMID 10447910
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- 1. South Med J. 2002 Jul;95(7):753-5. Beals-Hecht syndrome. Jones JL, Lane JE, Logan JJ, Vanegas ME. Beals-Hecht syndrome, also known as congenital contractural arachnodactyly, is caused by a defect in fibrillin as ...
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