hereditary ovalocytosis

遺伝性楕円赤血球症

関

hereditary elliptocytosis

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1. 世襲の,親譲りの / 遺伝的な,遺伝性の

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• 1. 遺伝性楕円赤血球症：臨床的特徴および診断 hereditary elliptocytosis clinical features and diagnosis
• 2. 赤血球表面抗原および細胞骨格蛋白質の異常によるマラリアに対する防御 protection against malaria by abnormalities in red cell surface antigens and cytoskeletal proteins
• 3. 遺伝性楕円赤血球症：遺伝学と病因 hereditary elliptocytosis genetics and pathogenesis
• 4. 腎尿細管性アシドーシスの病態生理およびカリウムバランスへの影響 pathophysiology of renal tubular acidosis and the effect on potassium balance
• 5. 末梢血塗抹標本の評価 evaluation of the peripheral blood smear

English Journal

• ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders.

• King MJ1, Garçon L, Hoyer JD, Iolascon A, Picard V, Stewart G, Bianchi P, Lee SH, Zanella A; International Council for Standardization in Haematology.
• International journal of laboratory hematology.Int J Lab Hematol.2015 Mar 18. doi: 10.1111/ijlh.12335. [Epub ahead of print]
• INTRODUCTION: Hereditary spherocytosis (HS), hereditary elliptocytosis (HE), and hereditary stomatocytosis (HSt) are inherited red cell disorders caused by defects in various membrane proteins. The heterogeneous clinical presentation, biochemical and genetic abnormalities in HS and HE have been well
• PMID 25790109

• Evaluating eosin-5-maleimide binding as a diagnostic test for hereditary spherocytosis in newborn infants.

• Christensen RD1, Agarwal AM2, Nussenzveig RH3, Heikal N2, Liew MA3, Yaish HM4.
• Journal of perinatology : official journal of the California Perinatal Association.J Perinatol.2014 Nov 6. doi: 10.1038/jp.2014.202. [Epub ahead of print]
• Objective:Neonates with undiagnosed hereditary spherocytosis (HS) are at risk for developing hazardous hyperbilirubinemia and anemia. Making an early diagnosis of HS in a neonate can prompt anticipatory guidance to prevent these adverse outcomes. A recent comparison study showed that a relatively ne
• PMID 25357094

• Biomechanical properties of red blood cells in health and disease towards microfluidics.

• Tomaiuolo G1.
• Biomicrofluidics.Biomicrofluidics.2014 Sep 17;8(5):051501. doi: 10.1063/1.4895755. eCollection 2014.
• Red blood cells (RBCs) possess a unique capacity for undergoing cellular deformation to navigate across various human microcirculation vessels, enabling them to pass through capillaries that are smaller than their diameter and to carry out their role as gas carriers between blood and tissues. Since
• PMID 25332724

Japanese Journal

• Molecular basis for membrane rigidity of hereditary ovalocytosis. A novel mechanism involving the cytoplasmic domain of band 3

• MOHANDAS N
• J Clin Invest 89, 686-692, 1992
• NAID 10011960153

• Hereditary ovalocytosis and reduced susceptibility to malaria in Papua New Guinea

• CATTANI J. A.
• Transactions of the Royal Society of Tropical Medicine and Hygiene 81, 705-709, 1987
• NAID 30009704537

Related Links

• Hereditary ovalocytosis - Drexel University College of Medicine

Definition Alternative Names Causes, incidence, and risk factors Symptoms Signs and tests Treatment Complications References Definition Hereditary ovalocytosis is rare condition passed down through families (inherited) in which ...

• Hereditary ovalocytosis - National Library of Medicine ...

Hereditary ovalocytosis is rare condition passed down through families (inherited) in which blood cells are slightly oval-shaped instead of round. It is a form of hereditary elliptocytosis. ... A.D.A.M., Inc. is accredited by ...

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★リンクテーブル★

リンク元	「遺伝性楕円赤血球症」
関連記事	「hereditary」

「遺伝性楕円赤血球症」

　　[★]

英

hereditary elliptocytosis, hereditary ovalocytosis

「hereditary」

　　[★]

• adj.

• 遺伝性の、遺伝の

関

heredity、heritable、inherit、inheritable、inheritable character、inheritance、inherited