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Congenital anemia
- Congenital dyserythropoietic anemia (CDA) is a rare group of inherited blood disorders that affects the development of red blood ... congenital CDA congenital dyserythropoietic anaemia ... Congenital dyserythropoietic anemia National Organization for Rare Disorders ( ...
- ... pure red cell aplasia DBA Erythrogenesis imperfecta Hypoplastic congenital anemia Inherited erythroblastopenia Pure hereditary red cell aplasia Genetic ...
- ... of Majeed syndrome is a blood disorder called congenital dyserythropoietic anemia. This disorder is one of many types of ... skin, and shortness of breath. The complications of congenital dyserythropoietic anemia can range from mild to severe.Some people ...
- ... not show signs and symptoms of the condition. Congenital spherocytic hemolytic anemia Congenital spherocytosis HS Spherocytic anemia Spherocytosis, type 1 ...
- ... CDAN1 gene have been identified in people with congenital dyserythropoietic anemia (CDA) type I. This condition is characterized by ... of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I. Blood. 2006 Jun 15;107(12): ...
- ... CDIN1 gene have been identified in people with congenital dyserythropoietic anemia (CDA) type I. This condition is characterized by ... Risco MB, Alonso-Dominguez JM, Moran-Jimenez MJ. Congenital dyserythropoietic anemia types Ib, II, and III: novel variants in ...
- ... KIF23 gene have been identified in people with congenital dyserythropoietic anemia (CDA) type III. This condition is characterized by ... Sandstrom H, Wahlin A, Mishima M, Golovleva I. Congenital dyserythropoietic anemia type III (CDA III) is caused by a ...
- ... SEC23B gene have been identified in people with congenital dyserythropoietic anemia (CDA) type II.This condition is characterized by ... SEC23B NCBI Gene ClinVar Denecke J, Marquardt T. Congenital dyserythropoietic anemia type II (CDAII/HEMPAS): where are we now? ...
- ... related immunodeficiency TRNT1-related immunodeficiency+ Genetic Testing Registry: Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome ...
- ... RACGAP1 gene have been identified in people with congenital dyserythropoietic anemia (CDA) type III. This condition is characterized by ... Mutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III. Haematologica. 2023 Feb 1;108(2): ...
