Diphosphoglycerate mutase deficiency of erythrocyte
Overview
Diphosphoglycerate mutase deficiency of erythrocyte: A rare inherited condition where a deficiency of an erythrocyte enzyme diphosphoglycerate mutase in red blood cells impairs the ability of red blood cells to deliver oxygen to body tissues that need it. In response, the body produces more red blood cells to assist oxygen delivery.
Symptoms
The list of signs and symptoms mentioned in various sources for Diphosphoglycerate mutase deficiency of erythrocyte includes the 2 symptoms listed below: * Cyanosis * Increased number of red blood cells
Causes
Cyanosis
Diagnosis
The signs and symptom information on this page attempts to provide a list of some possible signs and symptoms of Diphosphoglycerate mutase deficiency of erythrocyte. This medical information about signs and symptoms for Diphosphoglycerate mutase deficiency of erythrocyte has been gathered from various sources, may not be fully accurate, and may not be the full list of Diphosphoglycerate mutase deficiency of erythrocyte signs or Diphosphoglycerate mutase deficiency of erythrocyte symptoms. Furthermore, signs and symptoms of Diphosphoglycerate mutase deficiency of erythrocyte may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of any signs or symptoms and whether they are indeed Diphosphoglycerate mutase deficiency of erythrocyte symptoms.