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576 Possible Causes for ATRANSFERRINEMIA

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  • Congenital Liver Cirrhosis

    Management and treatment There is no cure for congenital atransferrinemia.[] ., Molecular characterization of a third case of human atransferrinemia. Blood. 104 , 2607 (2004)[] Genetic counseling Congenital atransferrinemia is inherited in an autosomal recessive manner and genetic counseling is available.[]

  • Microcytic Anemia

    The diagnosis of atransferrinemia was confirmed.[] Atransferrinemia Definition: Atranferrinemia is a genetic disorder wherein the plasma protein that carries iron (transferrin) in the blood stream is lacking.[] .  Increased requirements of iron (Pregnancy, Infancy, Lactation)  Inadequate presentation to erythroid precursors (Atransferrinemia, Atransferrin receptor antibodies) []

  • Red Blood Cell Disorder

    A Acute chest syndrome African iron overload Aldolase A deficiency Atransferrinemia B Bahima disease C Congenital dyserythropoietic anemia D Dyserythropoiesis E Eryptosis[]

  • Oculocutaneous Albinism Type 3

    […] albinism with congenital sensorineural deafness Oculocutaneous albinism type 1A Oculocutaneous albinism type 1B Temperature-sensitive oculocutaneous albinism type 1 Congenital atransferrinemia[]

  • Myelodysplasia

    Iron-transport deficiency anemia Iron-transport deficiency anemia (atransferrinemia) is exceedingly rare.[]

  • Hemosiderosis

    Atransferrinemia is characterized by anemia and hemosiderosis in the heart and liver. Mitral stenosis can also lead to pulmonary hemosiderosis .[] An absence of transferrin results from a rare genetic disorder known as atransferrinemia; a condition characterized by anemia and hemosiderosis in the heart and liver that[]

  • Calcinosis

    […] metabolism ( E83 , 275 ) Transition metal Fe excess: Primary iron overload disorder : Hemochromatosis/HFE1 Juvenile/HFE2 HFE3 African iron overload/HFE4 Aceruloplasminemia Atransferrinemia[]

  • African Iron Overload

    Iron Metabolism : Aceruloplasminemia, African Iron Overload, Atransferrinemia, Dps (DNA-Binding Proteins from Starved Cells), Ferritin, Average rating: 0 out of 5 stars, based[] […] disease nonalcoholic fatty liver disease following portocaval shunt dysmetabolic iron overload syndrome miscellaneous neonatal iron overload aceruloplasminemia congenital atransferrinemia[] X-linked sideroblastic anemia, enzyme deficiencies (pyruvate kinase; glucose-6-phosphate dehydrogenase) and very rare protein transport disorders aceruloplasminemia and atransferrinemia[]

  • Ophthalmoplegia totalis with Ptosis and Miosis

    There are two forms of this condition that cause an absence of transferrin in the affected individual: Acquired atransferrinemia Congenital atransferrinemia Contact the Genetic[] […] epilepsy - nephropathy [ ] Athyreosis [ ] ATIC deficiency [ ] Atkin-Flaitz syndrome [ ] ATLD [ ] ATMDS [ ] ATM/TM [ ] Atopic keratoconjunctivitis [ ] ATR-16 syndrome [ ] Atransferrinemia[] Atelosteogenesis, type III ( FLNB) Atelostogenesis, type I ( FLNB) Athabaskan brainstem dysgenesis syndrome ( HOXA1) Atopy ( SPINK5) ATP synthase deficiency, nuclear-encoded ( ATPAF2) Atransferrinemia[]

  • Aneurysm-Osteoarthritis Syndrome

    […] point mutation Brachydactyly - elbow wrist dysplasia Campomelic dysplasia Chronic intestinal pseudoobstruction Combined oxidative phosphorylation defect type 17 Congenital atransferrinemia[]

Further symptoms