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Inherited aplastic anemia
- ... People with this condition often also have physical abnormalities affecting various parts of the body.The RPL5 gene mutations that cause Diamond-Blackfan anemia are either inherited or occur early in development before birth, and ...
- ... have short stature, delayed sexual development, and skeletal abnormalities. Hereditary spherocytosis occurs in 1 in 2,000 individuals of Northern European ancestry. This condition is the most common cause of inherited anemia in that population. The prevalence of hereditary spherocytosis ...
- ... by blood cell disorders such as myeloma or aplastic anemia. Acquired factor VII deficiency can also be caused by certain ... Congenital factor VII deficiency is inherited in an autosomal recessive pattern, which means both ...
- ... RPS14 chromosome 5 ... Genetic Testing Registry: Myelodysplastic ...
- ... stiff and prone to rupture, leading to hemolytic anemia. Changes in the lipid composition of the membranes of red blood cells and ... This condition is inherited in an autosomal recessive pattern, which means both ...
- ... have been treated for another blood disease called aplastic anemia may develop PNH. In a small number of ... The spectrum of PIG-A gene mutations in aplastic anemia/paroxysmal nocturnal hemoglobinuria (AA/PNH): a high incidence ...
- ... decrease in the production of all blood cells (aplastic anemia). Affected individuals experience extreme tiredness (fatigue) due to ... and symptoms of the condition. Very rarely, Fanconi anemia is inherited in an autosomal dominant pattern or in an ...
- ... average chance of developing myelodysplastic syndrome (MDS) and aplastic anemia, which are disorders caused by abnormal blood stem ...
- ... red cell aplasia DBA Erythrogenesis imperfecta Hypoplastic congenital anemia Inherited erythroblastopenia Pure hereditary red cell aplasia Genetic Testing ...
- ... The spectrum of PIG-A gene mutations in aplastic anemia/paroxysmal nocturnal hemoglobinuria (AA/PNH): a high incidence ...