16+ Pyruvate Kinase Deficiency Hemolytic Anemia US. Pyruvate kinase (pk) deficiency is the most frequent cause of congenital nonspherocytic hemolytic anemia with a prevalence estimated at 1/20,000 in the general white population. It is caused by mutations in the pklr gene.
(PDF) Hemolytic anemia caused by hereditary pyruvate ... from i1.rgstatic.net Not having enough of this enzyme causes red blood cells to break down easily. Pyruvate kinase (pk) deficiency is a rare inherited disease that causes a lifelong condition called hemolytic anemia, a certain type of anemia where the body destroys red blood cells, as well as other serious complications. The anemia is intermittent, the age of onset is variable, and clinical signs are also variable.
Hereditary nonspherocytic anemias are rare genetic conditions that affect the red blood cells.
Erythrocyte pyruvate kinase deficiency mutation identified in multiple breeds of domestic cats. Not having enough of this enzyme causes red blood cells to break down easily. Pyruvate kinase (pk) deficiency is the most common cause of hereditary nonspherocytic hemolytic anemia. Consensus recommendations on the diagnosis of pyruvate kinase deficiency.
Berbagi
Posting Komentar
untuk "16+ Pyruvate Kinase Deficiency Hemolytic Anemia US"
Posting Komentar untuk "16+ Pyruvate Kinase Deficiency Hemolytic Anemia US"