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296 Possible Causes for Autosomal Recessive, Hemoglobin Decreased, 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[ncbi.nlm.nih.gov] All experienced an increase in hemoglobin and decrease in reticulocyte count early after LPS and at last follow-up. Twenty-two were sent for genetic analysis.[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]

  • 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[ncbi.nlm.nih.gov] Abstract Sideroblastic anemias are acquired or inherited anemias that result in a decreased ability to synthesize hemoglobin in red blood cells and result in the presence[ncbi.nlm.nih.gov] The characteristic hypochromic, microcytic anemia typically becomes manifest in the first three decades of life.[ncbi.nlm.nih.gov]

  • Thalassemia

    Abstract β-Thalassemia (β-thal) is the most widespread autosomal recessive disorder worldwide.[ncbi.nlm.nih.gov] Clinical Information A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains.[icd9data.com] 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] , decreased mean corpuscular volume (MCV) and decreased mean corpuscular hemoglobin (MCH) Essential features Group of inherited autosomal recessive diseases caused by an α-globin[pathologyoutlines.com] MATERIAL AND METHODS: Two hundred six patients with hypochromic microcytic anemia were evaluated for alpha thalassemia.[ncbi.nlm.nih.gov]

  • Iron Deficiency Anemia

    Iron-refractory iron deficiency anemia (IRIDA) is a rare hereditary form of IDA with autosomal recessive inheritance.[ncbi.nlm.nih.gov] Although the risk of GI cancer (GIC) increases as hemoglobin decreases, guidelines do not usually recommend hemoglobin thresholds for IDA investigation.[ncbi.nlm.nih.gov] Abstract Iron-refractory iron deficiency anemia (IRIDA) is a rare autosomal recessive disease characterized by congenital hypochromic microcytic anemia, low transferrin saturation[ncbi.nlm.nih.gov]

  • 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] Males affected with sideroblastic anemia had growth retardation, hypochromic microcytic anemia, elevated serum iron, decreased unsaturated iron-binding capacity, increased[ncbi.nlm.nih.gov] Hypochromic microcytic anemias include: Iron deficiency anemia: The most common cause of microcytic anemia is an iron deficiency in the blood.[healthline.com]

  • Cooley's Anemia

    recessive trait requiring that both parents pass on a copy of the defective gene located on the chromosome numbered 11.[merriam-webster.com] Cooley's anemia disease causes a dramatic decrease in the production of hemoglobin, resulting in anemia. This anemia can cause people to be more tired than normal.[dshs.state.tx.us] The defective gene in Cooley's anemia is on chromosome 11. The insufficient production of the globin chains results in microcytic anemia.[symptoma.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] It is defined by abnormally low hemoglobin concentration or decreased red blood cells. Several classification systems exist.[ncbi.nlm.nih.gov] The anemia is then categorized as microcytic, macrocytic or normocytic, with or without reticulocytosis.[ncbi.nlm.nih.gov]

  • Megaloblastic Anemia

    The mode of inheritance follows an autosomal recessive pattern and the syndrome was completely reversed by parentral vitamin B12 therapy.[ncbi.nlm.nih.gov] Last updated Nov. 17, 2018 Megaloblastic Anemia is a type of anemia (decrease in red blood cell, decrease in hemoglobin in red blood cell, or decrease in blood volume).[dovemed.com] Recently, she presented with microcytic anemia, and iron deficiency anemia was diagnosed initially.[ncbi.nlm.nih.gov]

  • Thalassemia Minor

    Editor’s Note: From Wikipedia – “Thalassaemia or “thalassemia” is an inherited autosomal recessive blood disease.[osseonews.com] Hemoglobin levels may be slightly decreased but with little clinical consequence. A person with beta thalassemia minor has a normal life expectancy.[labce.com] Abstract Iron deficiency anemia (IDA) and thalassemia minor are two of the most common causes of microcytic anemias worldwide.[ncbi.nlm.nih.gov]

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