- 同
- CMFTD
WordNet
- write by means of a keyboard with types; "type the acceptance letter, please" (同)typewrite
- a small metal block bearing a raised character on one end; produces a printed character when inked and pressed on paper; "he dropped a case of type, so they made him pick them up"
- (biology) the taxonomic group whose characteristics are used to define the next higher taxon
- a subdivision of a particular kind of thing; "what type of sculpture do you prefer?"
- all of the tokens of the same symbol; "the word `element contains five different types of character"
- printed characters; "small type is hard to read"
- identify as belonging to a certain type; "Such people can practically be typed" (同)typecast
- make ones way by force; "He muscled his way into the office"
- animal tissue consisting predominantly of contractile cells (同)muscular_tissue
- one of the contractile organs of the body (同)musculus
- authority or power or force (especially when used in a coercive way); "the senators used their muscle to get the party leader to resign"
- tell a relatively insignificant lie; "Fibbing is not acceptable, even if you dont call it lying"
- a trivial lie; "he told a fib about eating his spinach"; "how can I stop my child from telling stories?" (同)story, tale, tarradiddle, taradiddle
- a slender and greatly elongated substance capable of being spun into yarn (同)fibre
- a leatherlike material made by compressing layers of paper or cloth (同)fibre, vulcanized fiber
- any of several elongated, threadlike cells (especially a muscle fiber or a nerve fiber) (同)fibre
- present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
PrepTutorEJDIC
- 〈C〉(…の)『型』,タイプ,類型,種類(kind)《+of+名》 / 〈C〉(その種類の特質を最もよく表している)『典型』,手本,模範《+of+名》 / 〈U〉《集合的に》活字;〈C〉(1個の)活字 / 〈U〉(印刷された)字体,活字 / 〈C〉(貨幣・メダルなどの)模様,図柄 / 〈C〉血液型(blood group) / …‘を'タイプに打つ / (…として)…‘を'分類する《+名+as+名(doing)》 / …‘の'型を決める / タイプライターを打つ
- 〈U〉(動物体の組織としての)『筋肉』,筋(きん);〈C〉(体の各部を動かす)筋肉 / 〈U〉力,(特に)筋力,腕力 / 《俗に》(…に)強引に割り込む《+『in on』(『into, through』)+『名』》
- (ささいな,罪のない)うそ / 軽いうそをつく
- (病気・身体的欠陥など)生まれつきの,先天的な
UpToDate Contents
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English Journal
- An adult with a rare form of congenital fiber type disproportion.
- Anandan C1, Milone M1.
- Muscle & nerve.Muscle Nerve.2017 Sep 7. doi: 10.1002/mus.25954. [Epub ahead of print]
- PMID 28881016
- Congenital fiber-type disproportion in an ambulatory rehabilitation setting : A case report.
- Palma S1, Keilani M1, Hasenoehrl T1, Ambrozy C1, Dana S1, Sycha T2, Crevenna R3.
- Wiener medizinische Wochenschrift (1946).Wien Med Wochenschr.2017 Jul 25. doi: 10.1007/s10354-017-0580-4. [Epub ahead of print]
- PMID 28744779
- A recessive mutation in beta-IV-spectrin (SPTBN4) associates with congenital myopathy, neuropathy, and central deafness.
- Knierim E1,2, Gill E1, Seifert F1, Morales-Gonzalez S1, Unudurthi SD3,4, Hund TJ3,4, Stenzel W5, Schuelke M6,7.
- Human genetics.Hum Genet.2017 Jul;136(7):903-910. doi: 10.1007/s00439-017-1814-7. Epub 2017 May 24.
- PMID 28540413
Japanese Journal
- 先天性筋線維タイプ不均等症からタイプ1線維優位先天性ミオパチーの病理像に変容した先天性ミオパチーの1例
- 柴田 理恵,草川 功,小澤 真津子,大矢 達男,埜中 征哉
- 脳と発達 30(4), 307-311, 1998
- 新生児期発症の先天性ミオパチーは重症で, 呼吸・嚥下障害を伴うことが多い. 我々は出生直後から呼吸管理を必要としたが栄養管理・感染のコントロールを行い, 1歳10カ月まで着実な発育が得られている1例を経験した. 中枢神経系の合併は頭蓋変形と軽微な精神遅滞のみである. 筋病理では, 生後1カ月時の筋生検で先天性筋線維タイプ不均等症の像を示したが, 生後1年目の筋生検ではタイプ1線維優位先天性ミオパチ …
- NAID 130004183257
- 著明な顔面筋り患を伴った先天性筋線維タイプ不均等症の1例
- 志倉 圭子
- 脳と発達 18(1), 72-74, 1986
- … り暗泣や笑いなどの表情がほとんど確認できないほど著明な顔面筋罹患と, 全身の筋力低下を伴った精神運動発達遅滞の女児に, 筋組織検査を施行したところ, タイプ1線維萎縮・タイプ1線維優位の傾向・タイプ2C線維の残存 (13.5%) を示す先天性筋線維タイプ不均等症 (congenital fiber typedisproportion (CFTD)) の所見を得た.臨床経過として精神運動発達の獲得に比し顔面筋罹患の改善はほとんどみられなかった. …
- NAID 130004182207
- 生検筋でFiber type disproportionを呈したMultiple sulfatase deficiencyの1例
- 舘 延忠,藤林 伸助,我妻 浩治,南 良二,今村 重孝
- 脳と発達 16(3), 205-209, 1984
- … e染色にてtype I線維の萎縮, type I線維predominanceを認め, fider typedisproportionを示したが, 腓腹神経に認められた脱髄所見に対応するgroupatrophy, small angulated fibers等は認められなかった.患児は, 膝関節が拘縮し, 固定によりfiber typedi sproportionの所見を呈したことも否定できないが, MSDにおける脱髄過程が, fiber type disproportionを生じる …
- NAID 130004182071
Related Links
- Congenital fiber-type disproportion is a condition that primarily affects skeletal muscles, which are muscles used for movement. People with this condition typically experience muscle weakness (myopathy), particularly in ...
- Congenital fiber type disproportion (CFTD) is a rare genetic muscle disease that is usually apparent at birth (congenital myopathy). It belongs to a group of muscle conditions called the congenital myopathies that tend to affect (. ...
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- 同
- congenital muscle fiber-type disproportion
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- (windows)ファイル内容表示(linux -> cat])
- ex. type report_20111118.jp.htm | php a.php > report_20111118.jp.jp.jp.html
- 関
- form、mode、pattern、type specimen、typed
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- 関
- congenital、congenitally
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- 関
- form、mode、pattern、type
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