小球性低色素性貧血
WordNet
- a deficiency of red blood cells (同)anaemia
- a lack of vitality (同)anaemia
- genus of terrestrial or lithophytic ferns having pinnatifid fronds; chiefly of tropical America (同)genus Anemia
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English Journal
- NCOA4 Deficiency Impairs Systemic Iron Homeostasis.
- Bellelli R1, Federico G1, Matte' A2, Colecchia D3, Iolascon A4, Chiariello M3, Santoro M1, De Franceschi L2, Carlomagno F5.
- Cell reports.Cell Rep.2016 Jan 26;14(3):411-21. doi: 10.1016/j.celrep.2015.12.065. Epub 2016 Jan 14.
- The cargo receptor NCOA4 mediates autophagic ferritin degradation. Here we show that NCOA4 deficiency in a knockout mouse model causes iron accumulation in the liver and spleen, increased levels of transferrin saturation, serum ferritin, and liver hepcidin, and decreased levels of duodenal ferroport
- PMID 26776506
- Multiple copy number variants in a pediatric patient with Hb H disease and intellectual disability.
- Scheps KG1,2, Francipane L3, Nevado J4,5, Basack N6, Attie M6, Bergonzi MF3, Cerrone GE1,2, Lapunzina P4,5, Varela V1,2.
- American journal of medical genetics. Part A.Am J Med Genet A.2016 Jan 11. doi: 10.1002/ajmg.a.37532. [Epub ahead of print]
- Two distinct syndromes that link α-thalassemia and intellectual disability (ID) have been described: ATR-X, due to mutations in the ATRX gene, and ATR-16, a contiguous gene deletion syndrome in the telomeric region of the short arm of chromosome 16. A critical region where the candidate genes for t
- PMID 26753516
- Point mutations which should not be overlooked in Hb H disease.
- Farashi S1,2, Bayat N2, Vakili S2, Faramarzi Garous N2, Ashki M2, Imanian H2, Najmabadi H1,2, Azarkeivan A1,3.
- Expert review of hematology.Expert Rev Hematol.2016 Jan;9(1):107-13. doi: 10.1586/17474086.2016.1107470. Epub 2015 Nov 2.
- BACKGROUND: Hb H disease is an alpha-thalassemia (α-thal) syndrome characterized by chronic hemolytic anemia that occurs when three of total four α-globin genes lost their function due to completely deletions or different kind of mutations.OBJECTIVE: We here described 66 patients who have been dia
- PMID 26523940
Japanese Journal
- 慢性閉塞性呼吸器疾患の男性患者に発症したアルコール依存関連鉄芽球性貧血の1例
- 大野 仁嗣
- 天理医学紀要 16(1), 25-30, 2013
- 症例は69歳の男性. かねてより慢性閉塞性呼吸器疾患のため治療を受けていたところ, 小球性・低色素性貧血を認めたため紹介を受けた. 血液検査では, ヘモグロビン値7.6 g/dL, 平均赤血球容積70 fL, 平均赤血球血色素量21.1 pg, 平均赤血球血色素濃度30.3%であった. 血清鉄233 μg/dL, 総鉄結合能265 μg/dL, トランスフェリン飽和度87.9%, フェリチン55 …
- NAID 130004676046
- p,p′-DDT induces microcytic anemia in rats
- Tomita Mariko,Yoshida Toshinori,Fukumori Junko,Yamaguchi Satoru,Kojima Sayuri,Fukuyama Tomoki,Ohnuma-Koyama Aya,Takahashi Naofumi,Takeuchi-Kashimoto Yukiko,Kuwahara Maki,Nakashima Nobuaki,Ohtsuka Ryoichi,Takeda Makio,Kosaka Tadashi,Harada Takanori
- The Journal of Toxicological Sciences 38(5), 775-782, 2013
- … Emerging evidence suggests that chronic exposure to DDT and its derivatives is associated with a variety of human disorders such as anemia. … The present study demonstrated that p,p′-DDT caused microcystic anemia in a dose-dependent manner (0, 5, 50, and 500 ppm) in the long-term study up to 2 years. …
- NAID 130004447078
Related Links
- Microcytic hypochromic anemia: Introduction Microcytic hypochromic anemia: Microcytic anemia is a blood disorder characterized by small red blood cells (erythrocytes) which have insufficient haemoglobin and hence have a reduced ...
- 1. Med Clin North Am. 1992 May;76(3):549-66. Microcytic anemia. Differential diagnosis and management of iron deficiency anemia. Massey AC(1). Author information: (1)Department of Internal Medicine, University of ...
★リンクテーブル★
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- 英
- microcytic hypochromic anemia
- 同
- 低色素性小球性貧血？？？
- 関
- 貧血、小球性貧血
[show details]
検査値
貧血
- 原発性(先天性、獲得性)
- 二次性
- ピリドキシン反応性
鉄剤が無効な代表的な小球性低色素性貧血
[★]
- 関
- hypochromia