WordNet
- having or involving or consisting of more than one part or entity or individual; "multiple birth"; "multiple ownership"; "made multiple copies of the speech"; "his multiple achievements in public life"; "her multiple personalities"; "a pineapple is a multiple fruit"
- the product of a quantity by an integer; "36 is a multiple of 9"
- present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
PrepTutorEJDIC
- 多数の部分(要素)から成る,複合の,複式の / 倍数
- (病気・身体的欠陥など)生まれつきの,先天的な
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. 新生児における筋緊張低下を引き起こす末梢神経および筋肉の障害に関する概要 overview of peripheral nerve and muscle disorders causing hypotonia in the newborn
- 2. 脊髄性筋萎縮症 spinal muscular atrophy
- 3. 新生児および幼児における神経筋接合部障害 neuromuscular junction disorders in newborns and infants
- 4. 先天性ミオパシー congenital myopathies
- 5. 羊水過多 polyhydramnios
English Journal
- Failed caudal block due to physiologic changes associated with a cerebrospinal fluid leak: a case report.
- Bruce E1, Spencer AO2, Albayram MS3.
- Canadian journal of anaesthesia = Journal canadien d'anesthesie.Can J Anaesth.2016 May;63(5):603-607. Epub 2016 Jan 12.
- PURPOSE: The sum of the volumes of brain tissue, cerebrospinal fluid (CSF), and intracranial blood remain constant. This tenet of the Monroe-Kellie hypothesis is most often considered in the setting of intracranial hypertension, but it can also be applied in the setting of CSF volume depletion. We u
- PMID 26759160
- Novel VIPAS39 mutation in a syndromic patient with arthrogryposis, renal tubular dysfunction and intrahepatic cholestasis.
- Aflatounian M1, Smith H2, Farahani F1, Tofighi Naeem A1, Straatman-Iwanowska A2, Zoghi S3, Khatri U2, Tajdini P1, Fallahi GH1, Gissen P2, Rezaei N4.
- European journal of medical genetics.Eur J Med Genet.2016 Apr;59(4):237-9. doi: 10.1016/j.ejmg.2016.01.005. Epub 2016 Jan 23.
- ARC syndrome is a rare autosomal recessive disease, characterized by arthrogryposis, renal tubular dysfunction and cholestasis. Herein a 2.5 month old infant with dysmorphic features, including small anterior fontanel, low set ears, beaked nose and high arched palate is presented who was referred be
- PMID 26808426
- The clubfoot painted by Jusepe de Ribera: a controversial diagnosis.
- Stahl A1, Tourame P1,2, Montjean D2.
- The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.J Matern Fetal Neonatal Med.2016 Apr;29(8):1308-10. doi: 10.3109/14767058.2015.1046829. Epub 2015 Sep 28.
- The Clubfoot painted by José de Ribera depicts a young beggar affected by a typical equinus clubfoot. He shows a contorted right hand and wrist. His left hand holds a begging note, suggesting some difficulty to speak. This condition may be caused by a cerebral palsy, consisting of a brain injury in
- PMID 26414783
Japanese Journal
- A Case of Tracheotomy in a Patient with Pena-Shokeir Syndrome Type I
- Yoshida Saeko,Moriai Shigetaka,Wada Tetsuji,Kanai Naoki
- 耳鼻咽喉科臨床 補冊 140(0), 110-111, 2014
- … This disease is characterized by congenital multiple arthrogryposis, characteristic facial anomalies, and pulmonary hypoplasia. …
- NAID 130004707410
- Pena-Shokeir症候群I型の気管切開例
- 吉田 沙絵子,森合 重誉,和田 哲治 [他],金井 直樹
- 耳鼻咽喉科臨床 107(1), 71-75, 2014
- … This disease is characterized by congenital multiple arthrogryposis, characteristic facial anomalies, and pulmonary hypoplasia. …
- NAID 130003386118
- 先天性多数指屈曲拘縮例の母指および他の指の機能再建
- 森澤 妥,高山 真一郎,関 敦仁,日下部 浩,中川 敬介,松本 浩明
- 日本小児整形外科学会雑誌 = Journal of Japanese Paediatric Orthopaedic Association 18(1), 73-78, 2009-02-15
- NAID 10029266919
Related Links
- Arthrogryposis, also known as arthrogryposis multiplex congenita (AMC), is a rare congenital disorder that is characterized by multiple joint contractures and can include muscle weakness and fibrosis. It is a non-progressive disease.
- From 1975 to 2004 a total of 38 children handicapped by congenital multiple arthrogryposis were cared for. The congenital joint contractures demand a major effort in terms of surgical reconstruction. In the case of distal arthrogryposis the ...
Related Pictures
★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 | 「congenita」「multiple」「congenital」 |
「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
「congenita」
- adj.
- (後置するラテン語形容詞)先天性の
- ex.
「multiple」
- n.
- 倍数
- adj.
「congenital」
- adj.
- 生まれつきの、先天的な