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147 Possible Causes for Autosomal Recessive, Bone Marrow Biopsy Abnormal, Microcytic Anemia

  • 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] The characteristic hypochromic, microcytic anemia typically becomes manifest in the first three decades of life.[ncbi.nlm.nih.gov] We report the seventh case of autosomal recessive inherited mitochondrial myopathy, lactic acidosis, and sideroblastic anemia The patient, a product of consanguineous Persian[ncbi.nlm.nih.gov]

  • Thalassemia

    Abstract β-Thalassemia (β-thal) is the most widespread autosomal recessive disorder worldwide.[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] Congenital erythropoietic porphyria is a rare autosomal recessive disorder that affects heme-porphyrin synthesis.[ncbi.nlm.nih.gov]

  • Leukoerythroblastic Anemia

    Myeloproliferative Disease, Autosomal Recessive Myeloproliferative Disorder, Chronic, with Eosinophilia myeloproliferative neoplasm neonatal anemia normocytic anemia pancytopenia[rgd.mcw.edu] Biol Phys biopsy bleeding bleomycin bone marrow breast cancer cancer pain cancer patients cancer rehabilitation cancer treatment carcinoma chemotherapy chest chronic cisplatin[books.google.com] PH 1 is an autosomal recessive disorder characterized by hyperoxaluria, calcium oxalate urinary lithiasis in childhood, nephrocalcinosis and renal failure which in turn leads[ijpmonline.org]

  • Paroxysmal Nocturnal Hemoglobinuria

    recessive inheritance with incomplete penetrance.22 In a family having 1 sibling with a PDA, there is an 3% chance of a PDA in a subsequent offspring.21 The precise mechanisms[ahajournals.org] […] the requirement of genetic predisposition and an environmental trigger that occurs at a vulnerable time.21 The genetic mechanism of patent ductus in some patients may be autosomal[ahajournals.org]

  • Iron Deficiency Anemia

    Iron-refractory iron deficiency anemia (IRIDA) is a rare hereditary form of IDA with autosomal recessive inheritance.[ncbi.nlm.nih.gov] A small amount of bone marrow fluid (aspiration) or solid bone marrow tissue (called a core biopsy) are taken. These are often taken from the hip bones.[massgeneral.org] 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]

  • 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] In childhood, in the setting of hypocellular bone marrow with absence of cytogenetic abnormality [ 4 ] or a bone marrow biopsy with topography and cellularity of the local[intechopen.com] Causes of Microcytic Anemia Is It Anemia? Is It Microcytic?[pedsinreview.aappublications.org]

  • Alpha-Thalassemia

    The mode of transmission of alpha thalassaemia is autosomal recessive.[ncbi.nlm.nih.gov] marrow biopsy : reactive hyperplasia Confirmatory tests Hb-electrophoresis Alpha thalassemia can usually only be detected if 3 alleles are defective.[amboss.com] MATERIAL AND METHODS: Two hundred six patients with hypochromic microcytic anemia were evaluated for alpha thalassemia.[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] Immunodeficiency. [89] Bone marrow biopsy pathology: Erythroid precursors featuring perinuclear mitochondrial iron deposits (“ringed sideroblasts”). [89] Search Keywords:[autoinflammatory-search.org] 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] Bone marrow aspiration and biopsy : This test can help determine whether cell production is happening normally in the bone marrow.[kidshealth.org] The defective gene in Cooley's anemia is on chromosome 11. The insufficient production of the globin chains results in microcytic anemia.[symptoma.com]

  • Acquired Sideroblastic Anemia

    This disease is inherited in autosomal recessive manner.[bloodgenetics.com] […] cells Ringed sideroblasts Cellular fragments Genetic studies of the relevant genes to detect abnormalities Bone marrow biopsy Flow cytometry analysis on bone marrow Many[dovemed.com] Miscellaneous disorders of bone marrow, including stromal and bone abnormalities. In: Foucar K (ed.)[nature.com]

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