Case 14-1968
- 4 April 1968
- journal article
- case report
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 278 (14) , 782-791
- https://doi.org/10.1056/nejm196804042781411
Abstract
Presentation of Case First admission. A twenty-one-year-old Italian man entered the hospital because of intermittent jaundice of long duration and recent dyspnea and ankle edema.For many years he had been aware of a yellow tint of his skin but had noticed no discoloration of the urine or stools. One month before entry there was the onset of swelling of the ankles and dyspnea on exertion.The patient's father had died as a result of leukemia. The diagnosis of thalassemia trait in his mother was subsequently made on the basis of typical blood morphology and an elevation of A2 . . .Keywords
This publication has 7 references indexed in Scilit:
- Thalassemia intermedia, with iron overload, cardiac failure, diabetes mellitus, hypopituitarism and porphyrinuriaThe American Journal of Medicine, 1967
- Thalassemia: The consequences of unbalanced hemoglobin synthesisThe American Journal of Medicine, 1966
- Cardiac Involvement in Cooley's AnemiaAnnals of the New York Academy of Sciences, 1964
- Pathology of the Cardiac Conduction System in HemochromatosisNew England Journal of Medicine, 1964
- FAMILIAL MEDITERRANEAN TARGET???OVAL CELL SYNDROMESThe Lancet Healthy Longevity, 1943
- ???TARGET CELL??? ANEMIAThe Lancet Healthy Longevity, 1940
- ANEMIA IN CHILDRENAmerican Journal of Diseases of Children, 1927