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Anemia
- ... leads to a blood disorder known as megaloblastic anemia. About half of affected individuals also have excess ... development of red blood cells, leading to megaloblastic anemia. In addition, low levels of vitamin B12 can ...
- ... hydrops fetalis), a shortage of red blood cells (anemia), and an enlarged liver and spleen (hepatosplenomegaly). HbH ... HbH disease is characterized by mild to moderate anemia, hepatosplenomegaly, and yellowing of the eyes and skin ( ...
- ... glutamate formiminotransferase deficiency is also characterized by megaloblastic anemia. Megaloblastic anemia occurs when a person has a low number of red blood cells (anemia), and the remaining red blood cells are larger ...
- ... characterized by a condition known as chronic hemolytic anemia, in which red blood cells are broken down (undergo hemolysis) prematurely. Chronic hemolytic anemia can lead to unusually pale skin (pallor), yellowing ...
- ... also usually have a condition known as hemolytic anemia, in which red blood cells are broken down ( ... resulting in a shortage of red blood cells (anemia). Anemia can cause pale skin, weakness, fatigue, and ...
- ... individuals usually develop a blood disorder called megaloblastic anemia. Megaloblastic anemia occurs when a person has a low number of red blood cells (anemia), and the remaining red blood cells are larger ...
- ... due to low numbers of red blood cells (anemia), frequent infections due to low numbers of white ... NU. Ataxia-pancytopenia: syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous leukemia. Cancer Genet ...
- ... with homocystinuria develop a blood disorder called megaloblastic anemia. Megaloblastic anemia occurs when a person has a low number of red blood cells (anemia), and the remaining red blood cells are larger ...
- ... Health Condition MedlinePlus Genetics provides information about Fanconi anemia More About This Health Condition Inherited mutations in ... PubMed BRCA2 DNA REPAIR-ASSOCIATED PROTEIN; BRCA2 FANCONI ANEMIA, COMPLEMENTATION GROUP D1; FANCD1 NCBI Gene ClinVar Chen ...
- ... also called familial hyperinsulinism Familial Mediterranean fever Fanconi anemia GRACILE syndrome Gaucher disease Glycogen storage disease type ... disease Sickle cell disease , also called sickle cell anemia Sjögren-Larsson syndrome Tay-Sachs disease Tyrosinemia Usher ...