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686 Possible Causes for Autosomal Recessive, Hemolytic Anemia, Microcytic Anemia

  • Erythropoietic Protoporphyria

    […] effect from the mutant FECH allele. 25 The prevalence of autosomal recessive EPP has not been established.[jmg.bmj.com] anemia, and splenomegaly.[icd10data.com] Microcytic anemia occurs in 20% to 60% of patients. We investigated 178 patients with dominant EPP confirmed by molecular analysis.[ncbi.nlm.nih.gov]

  • Hereditary Spherocytosis

    […] spherocytosis on repeated blood films, Coombs-negative hemolytic jaundice and normal MCHC and MCV measurements, where SDS-PAGE revealed alpha-spectrin deficiency, a rare autosomal-recessive[ncbi.nlm.nih.gov] Hereditary spherocytosis (HS) and pyruvate kinase (PK) deficiency are the most common causes of congenital hemolytic anemia.[ncbi.nlm.nih.gov] anemia of varying degree. [3] Uraninite is a radioactive, uranium-rich mineral and ore with a chemical composition that is largely UO2, but also contains UO3 and oxides of[interhomeopathy.org]

  • Thalassemia

    Abstract β-Thalassemia (β-thal) is the most widespread autosomal recessive disorder worldwide.[ncbi.nlm.nih.gov] We identified two causes of hemolytic anemia (congenital erythropoietic porphyria and alpha thalassemia) in this patient.[ncbi.nlm.nih.gov] Note : Thalassemia is a microcytic, hypochromic anemia. Its cause is a genetically based decreased synthesis of one or several globin chains.[lecturio.com]

  • Alpha-Thalassemia

    The mode of transmission of alpha thalassaemia is autosomal recessive.[ncbi.nlm.nih.gov] We report a case with hydrops fetalis resulting from homozygous alpha-thalassemia and alloimmune hemolytic anemia due to anti-JK3.[ncbi.nlm.nih.gov] MATERIAL AND METHODS: Two hundred six patients with hypochromic microcytic anemia were evaluated for alpha thalassemia.[ncbi.nlm.nih.gov]

  • Microcytic Anemia

    The objective of the study was to report a novel autosomal recessive lipodystrophy syndrome.[ncbi.nlm.nih.gov] PA Pernicious Anemia Medical » Physiology Rate it: IDA Iron Deficiency Anemia Medical » Physiology Rate it: AIHA Autoimmune Hemolytic Anemia Medical » Physiology Rate it:[abbreviations.com] Causes[edit] Typical causes of microcytic anemia include: Childhood Iron deficiency anemia,[1] by far the most common cause of anemia in general and of microcytic anemia in[en.wikipedia.org]

  • Hypochromic Microcytic Anemia with Iron Overload Type 2

    Severe congenital hypochromic anemia with ringed sideroblasts due to mutations in STEAP3 gene is most likely to be inherited in an autosomal recessive manner.[enerca.org] anemia Warm hemolytic anemia Microangiopathic hemolytic anemia Hereditary spherocytosis Autoimmune hemolytic anemia Severe burns Transfused RBC 's Slide Image of Hereditary[hematologylearning.weebly.com] Causes of Microcytic Anemia Is It Anemia? Is It Microcytic?[pedsinreview.aappublications.org]

  • Beta Thalassemia

    Thalassemia major and thalassemia intermedia are inherited in an autosomal recessive pattern, which means both copies of the HBB gene in each cell have mutations.[ghr.nlm.nih.gov] Beta thalassemia major causes hemolytic anemia, poor growth, and skeletal abnormalities during infancy.[ncbi.nlm.nih.gov] Note : Thalassemia is a microcytic, hypochromic anemia. Its cause is a genetically based decreased synthesis of one or several globin chains.[lecturio.com]

  • Hereditary Sideroblastic Anemia

    Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia. Nat Genet. 2009;41:651–3.[link.springer.com] ) Hemolytic anemia (Medical Encyclopedia) Iron deficiency anemia (Medical Encyclopedia) Pernicious anemia (Medical Encyclopedia) Vitamin B12 level (Medical Encyclopedia) [[icdlist.com] Hypochromic microcytic anemias include: Iron deficiency anemia: The most common cause of microcytic anemia is an iron deficiency in the blood.[healthline.com]

  • Anemia

    ORPHA:1047 Synonym(s): - Prevalence: Unknown Inheritance: Autosomal dominant or Autosomal recessive or X-linked recessive or X-linked dominant or Mitochondrial inheritance[orpha.net] Anyone of any age can develop hemolytic anemia.[healthline.com] The anemia is then categorized as microcytic, macrocytic or normocytic, with or without reticulocytosis.[ncbi.nlm.nih.gov]

  • Constitutional Megaloblastic Anemia due to Folate Metabolism Disorder

    Affiliated tissues include neutrophil , and related phenotypes are jaundice and pallor OMIM : 57 Dihydrofolate reductase deficiency is an autosomal recessive metabolic disorder[malacards.org] anemias D589Hereditary hemolytic anemia, unspecified D590Drug-induced autoimmune hemolytic anemia D591Other autoimmune hemolytic anemias D592Drug-induced nonautoimmune hemolytic[cms.gov] […] by severe microcytic anemia, B-cell lymphopenia, panhypogammaglobulinemia, and variable neurodegeneration.[bloodgenetics.com]

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