遺伝性糸球体疾患
WordNet
- receive from a predecessor; "The new chairman inherited many problems from the previous chair"
- obtain from someone after their death; "I inherited a castle from my French grandparents"
- receive by genetic transmission; "I inherited my good eyesight from my mother"
- an impairment of health or a condition of abnormal functioning
- caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological
- of or relating to glomeruli
PrepTutorEJDIC
- (…から)〈財産・権利・称号など〉‘を'『相続する』《+『名』+『from』+『名』》 / (…から)〈体質・性質など〉‘を'『受け継ぐ』《+『名』+『from』+『名』》 / (前任者・前代から)…‘を'受け継ぐ,継承ぐ,継承する《+『名』+『from』+『名』》 / 財産を相続する
- (体の)『病気』,疾患 / (精神・道徳などの)病気,病弊
- 女性の話術芸人 =diseur
- 病気にかかった / 病的な,不健全な(morbid)
UpToDate Contents
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English Journal
- Nephrotic syndrome and thrombotic microangiopathy caused by cobalamin C deficiency.
- Koenig JC1, Rutsch F, Bockmeyer C, Baumgartner M, Beck BB, Kranz B, Konrad M.
- Pediatric nephrology (Berlin, Germany).Pediatr Nephrol.2015 Jul;30(7):1203-6. doi: 10.1007/s00467-015-3110-x. Epub 2015 Apr 18.
- BACKGROUND: Cobalamin C (CblC) defects are inherited autosomal recessive disorders of vitamin B12 metabolism due to mutations in the MMACHC gene. Renal manifestations include thrombotic microangiopathy (TMA), acute or chronic renal failure, tubulointerstitial nephritis, and proximal renal tubular ac
- PMID 25894566
- X-chromosome inactivation in female patients with Fabry disease.
- Echevarria L1,2, Benistan K2, Toussaint A3, Dubourg O4, Hagege AA5, Eladari D6, Jabbour F2, Beldjord C3, De Mazancourt P7, Germain DP1,2,7.
- Clinical genetics.Clin Genet.2015 May 14. doi: 10.1111/cge.12613. [Epub ahead of print]
- Fabry disease (FD) is an X-linked genetic disorder caused by the deficient activity of lysosomal α-galactosidase (α-Gal). While males are usually severely affected, clinical presentation in female patients may be more variable ranging from asymptomatic to, occasionally, as severely affected as mal
- PMID 25974833
- Podocyte p53 Limits the Severity of Experimental Alport Syndrome.
- Fukuda R1, Suico MA1, Kai Y1, Omachi K1, Motomura K1, Koga T2, Komohara Y3, Koyama K1, Yokota T1, Taura M1, Shuto T1, Kai H4.
- Journal of the American Society of Nephrology : JASN.J Am Soc Nephrol.2015 May 12. pii: ASN.2014111109. [Epub ahead of print]
- Alport syndrome (AS) is one of the most common types of inherited nephritis caused by mutation in one of the glomerular basement membrane components. AS is characterized by proteinuria at early stage of the disease and glomerular hyperplastic phenotype and renal fibrosis at late stage. Here, we show
- PMID 25967122
Japanese Journal
- Efficacy of 2-Hydroxypropyl-β-cyclodextrin in Niemann–Pick Disease Type C Model Mice and Its Pharmacokinetic Analysis in a Patient with the Disease
- Alport-leiomyomatosis症候群の1小児例
Related Links
- ... of patients, families and clinicians have led to the mapping and identification of numerous genetic loci involved in inherited glomerular disease and the functional characterization of their protein products. This information has 1 ...
- Hereditary glomerular disease Hereditary glomerular diseases are familial disorders of glomerular structure and function. Histomorphologically, there is disruption in one of the major components of the glomerulus, endothelial cells ...
★リンクテーブル★
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- 英
- inherited glomerular disease
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- 疾患:illnessより厳密な概念。「ある臓器に明確な障害が確認され、それによって症状が出ているとはっきり説明できる場合」 (PSY.9)
- 特定の原因、病態生理、症状、経過、予後、病理組織所見が全てそろった場合 (PSY.9)
- something that is very wrong with people's attitudes, way of life or with society.
- 関
- ail、ailment、disease entity、disorder、ill、illness、malady、sick、sickness
- disease ≠ illness ≠ disorder
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- 関
- glomeruli、glomerulus、kidney glomerulus、renal glomeruli、renal glomerulus
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- 関
- hereditary、heredity、inheritance
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- 関
- hereditary、heritable、inheritable、inheritable character