The laboratory diagnosis of megaloblastic anemias.
- 1 April 1978
- journal article
- review article
- Vol. 128 (4) , 294-304
Abstract
The diagnostic approach to megaloblastic anemia involves four usually sequential steps. The first step, recognition of megaloblastosis, requires attention to altered blood cell size and morphology. These changes may sometimes be subtle or masked. The cornerstone of the second step, identification of the specific vitamin deficiency, is assay of serum vitamin B(12) and folic acid levels, although they may occasionally be misleading. The third step, identification of the specific disease entity responsible for the vitamin deficiency, generally revolves around tests of absorption and gastric function. The fourth step, reevaluation after replacement therapy, is often not thought of as a diagnostic step but carries important diagnostic implications and is sometimes the only way in which coexisting abnormalities can be unmasked and identified.This publication has 100 references indexed in Scilit:
- Hereditary transcobalamin II deficiency: Clinical findings in a new familyThe Journal of Pediatrics, 1974
- DRUG‐INDUCED MALABSORPTION OF VITAMIN B12Acta Medica Scandinavica, 1974
- DRUG‐INDUCED MALABSORPTION OF VITAMIN B12Acta Medica Scandinavica, 1974
- Effect of Alcohol on Serum Folate LevelJournal of Clinical Investigation, 1973
- Vitamin B12levels in erythrocytes in hypochromic anaemiaJournal of Clinical Pathology, 1971
- Vitamin B12Levels in Erythrocytes in Anaemia due to Folate DeficiencyBritish Journal of Haematology, 1971
- Diagnostic value of the serum folate assayJournal of Clinical Pathology, 1971
- Effect of Steroids on Gastric Mucosal Structure and Function in Pernicious AnemiaActa Medica Scandinavica, 1967
- Aseptic addition method for Lactobacillus casei assay of folate activity in human serumJournal of Clinical Pathology, 1966
- The stomach in tropical sprue.Gut, 1965