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806 Possible Causes for Anemia, Erythropoietic Porphyria

  • Acute Hepatic Porphyria

    Four new chapters cover anemias unique to the newborn period, pathology of LHC and other histiocytic disorders, tumors of the spleen, and pathology and classification of myeloproliferative[books.google.com] porphyria E80.1 Porphyria cutanea tarda E80.2 Other and unspecified porphyria E80.20 Unspecified porphyria E80.21 Acute intermittent (hepatic) porphyria E80.3 Defects of[icd10data.com] Manifestations of porphyria include gastrointestinal, neurologic, and psychologic symptoms, cutaneous photosensitivity, pigmentation of the face (and later of the bones), and anemia[medical-dictionary.thefreedictionary.com]

  • Erythropoietic Porphyria

    anemia in a Kashmiri boy.[e-ijd.org] (disorder) Gunther disease Erythropoietic porphyria Congenital erythropoietic porphyria Uroporphyrinogen 3 Synthase Deficiency GC Günther disease PORPHYRIA, CONGENITAL ERYTHROPOIETIC[wikidata.org] Gov't MeSH terms 5-Aminolevulinate Synthetase/genetics* 5-Aminolevulinate Synthetase/metabolism Amino Acid Sequence Anemia, Sideroblastic/genetics Anemia, Sideroblastic/metabolism[ncbi.nlm.nih.gov]

  • Hepatoerythropoietic Porphyria

    68-year-old white man (Karnofsky score, 20) 2 with a 36-year history of porphyria and anemia was admitted for severe heart failure (left ventricular ejection fraction, 30[nejm.org] Erythropoietic porphyrias include erythropoietic protoporphyria and congenital erythropoietic porphyria.[ghr.nlm.nih.gov] Anemia was present in more than 50% of patients with HEP for whom hematologic status was reported (15 of 27), 2, 6 - 16, 19 - 22, 26, 28, 30, 32, 33 but severe anemia requiring[dx.doi.org]

  • Acute Intermittent Porphyria

    A Chinese female patient with very typical AIP symptoms of severe abdominal pain, seizures, hypertension, and tachycardia, accompanied with hyponatremia, anemia, and hyperbilirubinemia[ncbi.nlm.nih.gov] There are seven main types of porphyrias; acute intermittent porphyria and plumboporphyria are predominantly neuropsychiatric; congenital erythropoietic porphyria, porphyria[ncbi.nlm.nih.gov] The analysis of hematological and biochemical parameters during the second crisis showed anemia, leukocytosis, hyponatremia, mild hypokalemia, uremia and elevated C-reactive[ncbi.nlm.nih.gov]

  • Hemolytic Anemia

    , Hemolytic edit English hemolytic anemia form of anemia due to hemolysis haemolytic anaemia ANEMIA HEMOLYTIC secondary anemia from hemolysis Hemolytic Anemia Anemia, Hemolytic[wikidata.org] As a result, he was diagnosed as having Congenital erythropoietic porphyria.[ncbi.nlm.nih.gov] Low-grade hemolytic anemia occurs in 70% of prosthetic heart valve recipients, and severe hemolytic anemia occurs in 3%.[en.wikipedia.org]

  • Porphyria

    Sometimes the spleen must be removed in an attempt to treat the hemolytic anemia.[sciam.com] Desnick, Congenital erythropoietic porphyria: Recent advances, Molecular Genetics and Metabolism, 10.1016/j.ymgme.2018.12.008, (2018).[doi.org] LocusLink: Aminolevulinate, delta‐, synthase 2 (sideroblastic/hypochromic anemia) (ALAS2); MIM number: 301300. OMIM: ‐post/Omim/dispmim?[els.net]

  • Iron Deficiency

    […] did not reveal any findings indicating the cause of the anemia.[ncbi.nlm.nih.gov] Congenital erythropoietic porphyria (CEP) is an autosomal recessive disorder of heme synthesis characterized by reduced activity of uroporphyrinogen III synthase and the accumulation[ncbi.nlm.nih.gov] Go to Anemia, Sideroblastic Anemias, and Chronic Anemia for complete information on these topics.[emedicine.com]

  • Erythropoietic Protoporphyria

    The authors report a case of aplastic anemia in which refractory anemia, a subtype of myelodysplastic syndrome (MDS), developed 15 years after the onset and was subsequently[ncbi.nlm.nih.gov] Erythropoietic porphyrias include erythropoietic protoporphyria and congenital erythropoietic porphyria.[ghr.nlm.nih.gov] […] iron deficiency or the anemia of chronic disease (ACD).[ncbi.nlm.nih.gov]

  • Erythropoietic Coproporphyria

    Chronic transfusions for anemia will reduce erythropoiesis and porphyrin accumulation, whereas bone marrow transplantation can be curative.[ommbid.mhmedical.com] Prenatal exclusion of congenital erythropoietic porphyria (Günther's disease) in a fetus at risk. Hum. Genet. 53 (1980) 217–221 Google Scholar Doss, M.[link.springer.com] Molecular genetics of congenital erythropoietic porphyria.[ncbi.nlm.nih.gov]

  • Anemia

    Such types include sickle cell anemia, thalassemia and aplastic anemia. Anemia that results from aortic rupture has a very poor prognosis with about 80% mortality rate.[symptoma.com] Metabolic correction of congenital erythropoietic porphyria with iPSCs free of reprogramming factors. Am. J. Hum. Genet. 91, 109–121 (2012). 104.[dx.doi.org] Metabolic correction of congenital erythropoietic porphyria with iPSCs free of reprogramming factors.[ncbi.nlm.nih.gov]

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