Skupina vrozených hemolytických anemií, které jsou způsobeny defektní glykolýzou erytrocytů (bez nálezu defektního hemoglobinu nebo sférocytózy). Příčinou je většinou deficience enzymů glukóza-6-fosfátizomerázy, pyruvátkinázy a glukóza-6-fosfátdehydrogenázy.

Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. Common causes include deficiencies in GLUCOSE-6-PHOSPHATE ISOMERASE; PYRUVATE KINASE; and GLUCOSE-6-PHOSPHATE DEHYDROGENASE.

DUI

D000746 MeSH Prohlížeč

CUI

M0001130

Historická pozn.

91(82)68; was see under ANEMIA, HEMOLYTIC, CONGENITAL 1982-90; was heading 1968-81; was ANEMIA, CONGENITAL NONSPHEROCYTIC HEMOLYTIC 1965-67

Online pozn.

use ANEMIA, HEMOLYTIC, CONGENITAL NONSPHEROCYTIC to search ANEMIA, CONGENITAL NON-SPHEROCYTIC HEMOLYTIC 1966-67

Veřejná pozn.

91,68; was see under ANEMIA, HEMOLYTIC, CONGENITAL 1982-90; was heading 1968-81; was ANEMIA, CONGENITAL NONSPHEROCYTIC HEMOLYTIC 1965-67