congenital microvillus atrophy

先天性微絨毛萎縮症

WordNet

1. a decrease in size of an organ caused by disease or disuse (同)wasting, wasting away
2. undergo atrophy; "Muscles that are not used will atrophy"
3. any weakening or degeneration (especially through lack of use) (同)withering
4. present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate

PrepTutorEJDIC

1. (栄養不良などによる)萎縮(いしゅく) / (一般的に)衰退,退化 / 萎縮する,衰退する / …'を'萎縮させる,衰退させる
2. (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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• 5. 先天性赤血球増多症および真性多血症の分子学的病因 molecular pathogenesis of congenital polycythemic disorders and polycythemia vera

English Journal

• Extraintestinal manifestations in an infant with microvillus inclusion disease: complications or features of the disease?

• Siahanidou T1, Koutsounaki E, Skiathitou AV, Stefanaki K, Marinos E, Panajiotou I, Chouliaras G.
• European journal of pediatrics.Eur J Pediatr.2013 Sep;172(9):1271-5. doi: 10.1007/s00431-013-1948-0. Epub 2013 Jan 25.
• Microvillus inclusion disease (MVID), a rare severe congenital enteropathy characterized by intracytoplasmic microvillous inclusions and variable brush border atrophy on intestinal epithelial cells histology, is associated with defective synthesis or abnormal function of the motor protein myosin Vb
• PMID 23354788

• MYO5B mutations in patients with microvillus inclusion disease presenting with transient renal Fanconi syndrome.

• Golachowska MR1, van Dael CM, Keuning H, Karrenbeld A, Hoekstra D, Gijsbers CF, Benninga MA, Rings EH, van Ijzendoorn SC.
• Journal of pediatric gastroenterology and nutrition.J Pediatr Gastroenterol Nutr.2012 Apr;54(4):491-8. doi: 10.1097/MPG.0b013e3182353773.
• BACKGROUND AND OBJECTIVE: : Microvillus inclusion disease (MVID) is a rare congenital enteropathy associated with brush border atrophy and reduced expression of enzymes at the enterocytes' apical surface. MVID is associated with mutations in the MYO5B gene, which is expressed in all epithelial tissu
• PMID 22441677

• Microvillous inclusion disease: a clinicopathologic study of 17 cases from the UK.

• Al-Daraji WI1, Zelger B, Zelger B, Hussein MR.
• Ultrastructural pathology.Ultrastruct Pathol.2010 Dec;34(6):327-32. doi: 10.3109/01913123.2010.500447.
• BACKGROUND: Microvillous inclusion disease (MVID) is a rare congenital disease producing intractable secretory diarrhea in early infancy. It is characterized by diffuse intestinal villous atrophy with no inflammatory reaction. Ultrastructural identification of apical microvillous inclusions in the s
• PMID 21070163

Japanese Journal

• Papadimitriou : Neonatal congenital microvillus atrophy

• Postgrad Med J 80, 80-83, 2004
• NAID 30021607421

Related Links

• Microvillus Inclusion Disease: Background, Pathophysiology ...

Microvillus inclusion disease (also referred to as congenital microvillus atrophy) is, with Tuft enteropathy, the best known disease of the intestinal epithelium causing intractable diarrhea of infancy, and a leading cause of ...

• Neonatal congenital microvillus atrophy - National Center for ...

Congenital microvillous atrophy (CMVA) is the leading cause of neonatal secretory diarrhoea with onset either in the first 72 hours of life (early onset) or at 6–8 weeks after birth (late onset). To date over 30 cases have been reported ...

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★リンクテーブル★

リンク元	「微絨毛封入体病」「先天性微絨毛萎縮症」
関連記事	「congenita」「microvillus」「congenital」「atrophy」

「微絨毛封入体病」

　　[★]

英

microvillus inclusion disease MVID

同

先天性微絨毛萎縮症 congenital microvillus atrophy、diarrhea 2, with microvillus atrophy diar2、Davidson disease、congenital familial protracted diarrhea with enterocyte brush-border abnormalities, intractable diarrhea of infancy

「先天性微絨毛萎縮症」

　　[★]

英

congenital microvillus atrophy

「congenita」

　　[★]

• adj.

• (後置するラテン語形容詞)先天性の

関

congenital、congenitally

• ex.

• dyskeratosis congenita、myotonia congenita

「microvillus」

　　[★]

微絨毛

関

microvillar、microvilli、microvillous

「congenital」

　　[★]

• adj.

• 生まれつきの、先天的な

　 　

「atrophy」

　　[★]

• n.

• 萎縮