びまん性メサンギウム硬化症
WordNet
- spread out; not concentrated in one place; "a large diffuse organization"
- move outward; "The soldiers fanned out" (同)spread, spread out, fan out
- lacking conciseness; "a diffuse historical novel"
- any pathological hardening or thickening of tissue (同)induration
- (of light rays) subjected to scattering by reflection from a rough surface or transmission through a translucent material; "diffused light"
- spreading by diffusion (同)diffusive, dispersive, disseminative
PrepTutorEJDIC
- 〈光・熱・液体など〉‘を'散らす,放散する,拡散させる / 〈学問・知識など〉‘を'広める,普及させる / 散る,放散する,拡散する / 広まる,普及する / 広く散った,広がった / 〈文体などが〉締まりのない,散漫な
- (組織・血管などの)硬化,硬化症
UpToDate Contents
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English Journal
- Respiratory-chain deficiency presenting as diffuse mesangial sclerosis with NPHS3 mutation.
- Baskin E, Selda Bayrakci U, Alehan F, Ozdemir H, Oner A, Horvath R, Vega-Warner V, Hildebrandt F, Ozaltin F.SourceDepartment of Pediatric Nephrology, Baskent University, Ankara, Turkey. esrabaskin@yahoo.com
- Pediatric nephrology (Berlin, Germany).Pediatr Nephrol.2011 Jul;26(7):1157-61. Epub 2011 Mar 2.
- Renal manifestations of mitochondrial cytopathies have been described, but nephrotic syndrome with respiratory-chain disorders have been described extremely rarely. We report a 9-month-old boy with a mitochondrial cytopathy preceded by a 2-month history of steroid-resistant nephrotic syndrome. Percu
- PMID 21365190
- Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome.
- Fencl F, Malina M, Stará V, Zieg J, Mixová D, Seeman T, Bláhová K.SourceDepartment of Pediatrics 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, V Úvalu 84, 150 06, Prague 5, Czech Republic, filip.fencl@gmail.com.
- European journal of pediatrics.Eur J Pediatr.2011 May 26. [Epub ahead of print]
- Congenital nephrotic syndrome (CNS) is a heterogeneous group of diseases with different causes and prognoses. Two thirds of cases of NS in the first year of life are caused by mutations in four genes (NPHS1, NPHS2, WT1, and LAMB2). The mutation of WT1 gene can lead to Denys-Drash syndrome (DDS). We
- PMID 21614510
Japanese Journal
- 中田 麻子,山藤 陽子,里村 憲一
- 日本小児腎臓病学会雑誌 = Japanese journal of pediatric nephrology 23(1), 35-39, 2010-04-15
- 今回われわれは，超低出生体重児が学校検尿にて蛋白尿を指摘された症例を経験したので報告する。 症例は9歳女児。在胎25週，出生体重624g，品体の第三子として出生。就学時健診にて蛋白尿をはじめて指摘された。9歳時に行った腎生検では細胞増殖や硬化病変は認めなかったが，糸球体面積が同年齢のそれに比較して増加していた。近年，低出生体重児が成人期に高血圧，耐糖能異常，脂質代謝異常，腎不全などさまざまな成人 …
- NAID 10026412131
- WT1遺伝子の変異を確認したびまん性メサンギウム硬化症の一例
- 澤井 俊宏,宗村 純平,澤井 ちひろ,西島 節子,岩井 勝,野村 康之,竹内 義博,川勝 秀一
- 日本小児腎臓病学会雑誌 18(1), 43-47, 2005
- 急激に進行するステロイド抵抗性のネフローゼ症候群として発症し，腎生検でびまん性メサンギウム硬化症（DMS）と診断し得た一例を経験した。本症例は，Wilms腫瘍抑制遺伝子（WT1）の変異がDenys-Drash症候群に特異的な部位に存在したことから不全型のDenys-Drash症候群と考えられた。乳幼児期に腎機能障害が急激に進行するステロイド抵抗性ネフローゼ症候群の症例ではDMSである可能性を考えて …
- NAID 130000077435
Related Links
- Discussion Diffuse mesangial sclerosis (DMS) was first described by Habib and Bios in 1973.[8] DMS is one of the causes for nephrotic syndrome (NS) that occurs more commonly in first two decades of life. It has a fatal course.
- Diffuse mesangial sclerosis symptoms, causes, diagnosis, and treatment information for Diffuse mesangial sclerosis (Mesangial sclerosis, diffuse) with alternative diagnoses, full-text book chapters, misdiagnosis, research treatments ...
- Go back to clinical information and images Diagnosis: Diffuse mesangial sclerosis The term diffuse mesangial sclerosis (DMS) indicates a characteristic glomerular histological alteration that occurs in childhood ...
★リンクテーブル★
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- 英
- diffuse mesangial sclerosis
- 関
- 糖尿病性腎症
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- 関
- diffusely、diffusion、diffusional、diffusive、disseminated、pervasive、spread、widespread
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- 関
- glomerular mesangium、mesangium