ぐにゃぐにゃ乳児
WordNet
- with a flopping sound; "he tumbled flop into the mud"
- the act of throwing yourself down; "he landed on the bed with a great flop" (同)collapse
- a complete failure; "the play was a dismal flop" (同)bust, fizzle
- someone who is unsuccessful (同)dud, washout
- fall loosely; "He flopped into a chair"
- fall suddenly and abruptly
- hanging limply; "a spaniel with floppy ears"
PrepTutorEJDIC
- ばったりと倒れる,どさりと腰かける / パタパタ動く / 《話》失敗する / …‘を'どさっと投げる / ばったり落ちる(倒れる)こと / どさっと落ちる音 / 《話》大失敗;失敗者
- (1歳未満の)『乳児』,乳飲み子 / 《英》(普通7歳未満の)学童 / 未成年者 / 幼児の,幼児用の / 始めたばかりの,初期の
- だらりと垂れた
UpToDate Contents
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English Journal
- Genetic evaluation of the floppy infant.
- Prasad AN, Prasad C.SourceDepartment of Pediatrics, University of Western Ontario, London, Ontario, Canada. narayan.prasad@lhsc.on.ca
- Seminars in fetal & neonatal medicine.Semin Fetal Neonatal Med.2011 Apr;16(2):99-108. doi: 10.1016/j.siny.2010.11.002. Epub 2010 Dec 4.
- Hypotonia in infants in the first year of life is a common diagnostic and management challenge for pediatricians and neonatologists. Several published clinical studies have shown that a substantial proportion of cases are accounted for by genetic disorders. Rapid advances in biotechnology, bioinform
- PMID 21131247
- Sequential neuroradiological and neurophysiological studies in a Japanese girl with merosin-deficient congenital muscular dystrophy.
- Fujii Y, Sugiura C, Fukuda C, Maegaki Y, Ohno K.SourceDepartment of Brain and Neurosciences, Tottori University, Yonago, Japan. yujinn0728@ybb.ne.jp
- Brain & development.Brain Dev.2011 Feb;33(2):140-4. doi: 10.1016/j.braindev.2010.02.003. Epub 2010 Mar 19.
- We describe the early manifestation and sequential assessment of the central and peripheral nervous system in a Japanese girl with merosin-deficient congenital muscular dystrophy. She showed severe hypotonia (floppy infant") and suffered mild respiratory failure postnatally. Serum creatine kinase
- PMID 20303224
- Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation.
- Tuppen HA, Fehmi J, Czermin B, Goffrini P, Meloni F, Ferrero I, He L, Blakely EL, McFarland R, Horvath R, Turnbull DM, Taylor RW.SourceMitochondrial Research Group, Institute for Ageing and Health, The Medical School, Newcastle University, Newcastle Upon Tyne NE2 4HH, UK.
- Molecular genetics and metabolism.Mol Genet Metab.2010 Aug;100(4):345-8. doi: 10.1016/j.ymgme.2010.04.010. Epub 2010 Apr 24.
- Mutations of the BCS1L gene are a recognised cause of isolated respiratory chain complex III deficiency and underlie several fatal, neonatal mitochondrial diseases. Here we describe a 20-year-old Kenyan woman who initially presented as a floppy infant but whose condition progressed during childhood
- PMID 20472482
Japanese Journal
- 急性硬膜外血腫後の高次脳機能障害と診断された筋強直性ジストロフィーの1例
- 庄 敦子,高野 真
- The Japanese Journal of Rehabilitation Medicine 49(10), 734-737, 2012
- … Severity of illness in DM patients varies from a floppy infant to a lack of awareness of the disease throughout one's lifetime. …
- NAID 130002079149
- フロッピーインファントにみられた粘膜下口蓋裂の1例
- 高田 佳之,小田 陽平,泉 直也,小林 正治,齊藤 力
- 日本口蓋裂学会雑誌 36(3), 208-212, 2011-10-25
- 今回,われわれは染色体異常のあるフロッピーインファントに粘膜下口蓋裂を合併したまれな症例を経験した。患者は10か月時にミルク摂取の際の鼻漏れを主訴に当科を初診した。粘膜下口蓋裂と二裂口蓋垂以外には明らかな外表奇形は無かったが,硬口蓋後方部に骨欠損を認めた。全身の筋力の低下があるものの呼吸困難は認めなかった。1歳6か月時に,当院小児科において精神運動発達遅滞を伴うフロッピーインファントとの診断を受け …
- NAID 10030795100
- 乳幼児健診で知っておくべき神経・筋疾患の知識 (特集 乳幼児健診とその周辺) -- (乳幼児健診の周辺の問題)
Related Links
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