Embden-Meyerhof defects

Embden-Meyerhof defects

[emb′den mī′ərhof]
Etymology: Gustav G. Embden, German biochemist, 1874-1933; Otto F. Meyerhof, German biochemist, 1884-1951
a group of hereditary hemolytic anemias caused by enzyme deficiencies. The most common form of the disorder is a pyruvate kinase deficiency. The condition is characterized by an absence of spherocytes and the presence of small numbers of crenated erythrocytes. The trait is transmitted as an autosomal-recessive gene, and the hemolytic anemia occurs only in homozygotes.