From Wikipedia, the free encyclopedia
Minkowski-Chauffard syndrome is a form of hemolytic anemia.[1]
It is named for Oskar Minkowski and Anatole Chauffard.[2]
[edit] See also
[edit] References
- ^ Mironchik EV, Dolgosheĭ TS, Liskovich TG, Madeshkina GA, Kokhkovski AB, Tyshchenko AD (2007). "[Long QT syndrome induced by cordaron and quinidine]" (in Russian). Klin Med (Mosk) 85 (3): 69–71. PMID 17523411.
- ^ synd/1685 at Who Named It
Pathology: hematology, hematologic disease (primarily D50-D77, 280-289) |
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RBCs/anemia/
hemoglobinopathy
(Myeloid) |
nutritional anemia: Iron deficiency anemia, Plummer-Vinson syndrome, Megaloblastic anemia ( Pernicious anemia)
hereditary hemolytic anemia: enzyme disorders ( G6PD Deficiency, Pyruvate kinase deficiency, Triosephosphate isomerase deficiency), Thalassemia, Sickle-cell disease/ trait, Hereditary spherocytosis, Hereditary elliptocytosis, Hereditary stomatocytosis
acquired hemolytic anemia: Autoimmune (Warm), HUS, MAHA, PNH, PCH
aplastic anemia: Acquired PRCA, Diamond-Blackfan anemia, Fanconi anemia • Sideroblastic anemia
Polycythemia - Methemoglobinemia
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Coagulation/platelets
(Myeloid) |
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Monocytes/Macrophages
(Myeloid) |
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Granulocytes
(Myeloid) |
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Other/general myeloid |
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Lymphoid |
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Other |
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