急性再発性ミオグロブリン尿症
WordNet
- of critical importance and consequence; "an acute (or critical) lack of research funds"
- having or demonstrating ability to recognize or draw fine distinctions; "an acute observer of politics and politicians"; "incisive comments"; "icy knifelike reasoning"; "as sharp and incisive as the stroke of a fang"; "penetrating insight"; "frequent penetrative observations" (同)discriminating, incisive, keen, knifelike, penetrating, penetrative, piercing, sharp
- extremely sharp or intense; "acute pain"; "felt acute annoyance"; "intense itching and burning" (同)intense
- having or experiencing a rapid onset and short but severe course; "acute appendicitis"; "the acute phase of the illness"; "acute patients"
- of an angle; less than 90 degrees
- the presence of myoglobin in the urine
PrepTutorEJDIC
- (先の)『鋭い』,とがった / (痛み・感情などが)『激しい』,強い / (知力・感覚などが)『鋭い』,鋭敏な / (事態が)重大な / (病気が)急性の / (音が)高い,鋭い / 鋭角の
- 再発する;繰り返し起こる
UpToDate Contents
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English Journal
- An ignored cause of red urine in children: rhabdomyolysis due to carnitine palmitoyltransferase II (CPT-II) deficiency.
- Melek E, Bulut FD, Atmış B, Yılmaz BŞ, Bayazıt AK, Mungan NÖ.
- Journal of pediatric endocrinology & metabolism : JPEM.J Pediatr Endocrinol Metab.2017 Feb 1;30(2):237-239. doi: 10.1515/jpem-2016-0324.
- Carnitine palmitoyltransferase II (CPT-II) deficiency is an autosomal recessively inherited disorder involving the β-oxidation of long-chain fatty acids, which leads to rhabdomyolysis and subsequent acute renal failure. The clinical phenotype varies from a severe infantile form to a milder muscle f
- PMID 28085674
- McArdle Disease Misdiagnosed as Meningitis.
- Scalco RS1,2, Chatfield S1, Junejo MH3, Booth S1, Pattni J1, Godfrey R4, Quinlivan R1,5.
- The American journal of case reports.Am J Case Rep.2016 Nov 30;17:905-908.
- PMID 27899787
- Coexistence of VHL Disease and CPT2 Deficiency: A Case Report.
- Ferrara AM1, Sciacco M2, Zovato S1, Rizzati S1, Colombo I2, Boaretto F1, Moggio M2, Opocher G1,3.
- Cancer research and treatment : official journal of Korean Cancer Association.Cancer Res Treat.2016 Oct;48(4):1438-1442. Epub 2016 Mar 25.
- PMID 27034144
Related Links
- Recurrent myoglobinuria is characterized by recurrent attacks of rhabdomyolysis associated with muscle pain and weakness and followed by excretion of myoglobin in the urine. Renal failure may occasionally occur.
- Clinical test for Myoglobinuria, acute recurrent, autosomal recessive offered by Emory Genetics Laboratory ... Imported from OMIM Recurrent myoglobinuria is characterized by recurrent attacks of rhabdomyolysis ...
★リンクテーブル★
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- 英
- familial paroxysmal rhabdomyolysis
- 同
- 急性再発性横紋筋融解症 acute recurrent rhabdomyolysis、急性再発性ミオグロブリン尿症 acute recurrent myoglobinuria
- 関
- 横紋筋融解症
[★]
- 英
- acute recurrent myoglobinuria
- 関
- 家族性発作性横紋筋融解症
[★]
- (疾患)急性の、急性型の、急性的な。(形状が)鋭い、鋭角の。(感覚、才知などが)鋭い。明敏な、鋭い眼識のある。
- 関
- acutely、quick、sharp
[★]
- 関
- iterative、recurrence、recurrently、regression、relapsing、repetitive