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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Anemia, Hemolytic, Congenital > Anemia, Dyserythropoietic, Congenital
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Anemia > Anemia, Hemolytic > Anemia, Hemolytic, Congenital > Anemia, Dyserythropoietic, Congenital

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Anemia, Dyserythropoietic, Congenital  

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Tipo

  • mesh:Descriptor

Definición

  • A familial disorder characterized by ANEMIA with multinuclear ERYTHROBLASTS, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors (ERYTHROID PRECURSOR CELLS). Type II is the most common of the 3 types; it is often referred to as HEMPAS, based on the Hereditary Erythroblast Multinuclearity with Positive Acidified Serum test.

Concepto genérico

Etiquetas alternativas

  • Anemia, Congenital Dyserythropoietic
  • Congenital Dyserythropoietic Anemia
  • Dyserythropoietic Anemia, Congenital

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-F25P9R69-R

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RDF/XML TURTLE JSON-LD Creado 23/4/79, última modificación 8/7/13