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78 Possible Causes for Autosomal Recessive, Fainting Spells, Microcytic Anemia

  • 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[] 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[] This condition can also be inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations.[]

  • Sideroblastic Anemia

    Here, by positional cloning, we define a previously unknown form of autosomal recessive nonsyndromic congenital sideroblastic anemia, associated with mutations in the gene[] The characteristic hypochromic, microcytic anemia typically becomes manifest in the first three decades of life.[] We report the seventh case of autosomal recessive inherited mitochondrial myopathy, lactic acidosis, and sideroblastic anemia The patient, a product of consanguineous Persian[]

  • Microcytic Anemia

    The objective of the study was to report a novel autosomal recessive lipodystrophy syndrome.[] 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[] The mutation segregated in an autosomal-recessive fashion and was not detected in 275 unrelated ethnically matched healthy subjects.[]

  • Iron Deficiency Anemia

    Iron-refractory iron deficiency anemia (IRIDA) is a rare hereditary form of IDA with autosomal recessive inheritance.[] Abstract Iron-refractory iron deficiency anemia (IRIDA) is a rare autosomal recessive disease characterized by congenital hypochromic microcytic anemia, low transferrin saturation[] Abstract Iron-refractory iron deficiency anemia (IRIDA) is a rare autosomal-recessive disorder hallmarked by hypochromic microcytic anemia, low transferrin saturation, and[]

  • Hereditary Sideroblastic Anemia

    Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia. Nat Genet. 2009;41:651–3.[] Hypochromic microcytic anemias include: Iron deficiency anemia: The most common cause of microcytic anemia is an iron deficiency in the blood.[] recessive sideroblastic anemia Autosomal dominant aplasia and myelodysplasia Autosomal recessive sideroblastic anemia Blackfan-Diamond anemia Congenital amegakaryocytic thrombocytopenia[]

  • Acquired Sideroblastic Anemia

    This disease is inherited in autosomal recessive manner.[] We describe two cases of congenital sideroblastic anemia, one of them indicating an autosomal recessive inheritance, with their clinico-hematological profile.[] Anemia is usually microcytic in congenital sideroblastic anemia and macrocytic in acquired sideroblastic anemia.[]

  • Methylmalonic Acidemia with Homocystinuria Type cblF

    There are four types of the disease, all of which are inherited in an autosomal recessive manner and caused by functional deficiencies of methionine synthase and methylmalonyl-CoA[] Causes of Microcytic Anemia Is It Anemia? Is It Microcytic?[] It's a rare autosomal recessive disease in which there are several variants depending on the pathogenesis of the metabolic disorder (cblC, cblD, cblF and cblJ).[]

  • Anemia

    ORPHA:1047 Synonym(s): - Prevalence: Unknown Inheritance: Autosomal dominant or Autosomal recessive or X-linked recessive or X-linked dominant or Mitochondrial inheritance[] The anemia is then categorized as microcytic, macrocytic or normocytic, with or without reticulocytosis.[] Transmittance is autosomal recessive inheritance of abnormal GIF on chromosome arm 11q13.[]

  • Normocytic Normochromic Anemia

    Idiopathic - Anti-metabolites e.g. methotrexate, other cancer therapy - Alkylating agents e.g. cancer therapy - Virus e.g. parvovirus B19, EBV, HIV, HCV - Fanconi's anemia: autosomal[] anemia- iron deficiency, anemia of chronic disease, thalassemia minor, sideroblastic anemia Microcytic anemia 1.[] It is inherited as an autosomal dominant trait D. It is inherited as an autosomal recessive trait 14.[]

  • Unverricht-Lundborg Syndrome

    Unverricht disease, Unverricht syndrome (oon′fĕr-ikt″) [Heinrich Unverricht, Ger. physician, 1853–1912] A rare, fatal disease inherited as an autosomal recessive trait.[] ., what sorts of spells are likely to beset infants, children, or the elderly?[] anemia with liver iron overload Microdeletion 22q11.2 Microdeletion 9q22.3 Microdontia-type I microtia-deafness syndrome Microduplication 17p12 Microduplication Xp11.22p11.23[]

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