Fanconi's Anaemia. Simultaneous onset in 2 Siblings and unusual Cytological Findings
- 24 April 2009
- journal article
- case report
- Published by Wiley in Scandinavian Journal of Haematology
- Vol. 28 (5) , 431-440
- https://doi.org/10.1111/j.1600-0609.1982.tb00549.x
Abstract
Fanconi's anaemia is reported in 2 siblings. The simultaneous onset of pancytopenia after possible exposure to common external agents suggest that both a frail genotype and environmental factors may be etiologically involved in the disorder. One of the children died after having developed a monoblastic leukaemia. This patient disclosed very striking cytological abnormalities, including a dyserythropoietic pattern and ropalocytosis. The physiopathology of the latter abnormality, which has hitherto not been noticed in Fanconi's anaemia, is uncertain.Keywords
This publication has 11 references indexed in Scilit:
- Fanconi's anemia: terminal leukemia and “Forme fruste” in one familyClinical Genetics, 2008
- Formal genetics of Fanconi's anemiaHuman Genetics, 1976
- Fanconi anemia: Simultaneous onset of symptoms in two siblingsThe Journal of Pediatrics, 1976
- Multiple neoplasms in two siblings with a variant form of Fanconi's anemiaCancer, 1975
- Paroxysmal Cold Hemoglobinuria: Transmission and Scanning Electron Microscopy Features of ErythrocytesAmerican Journal of Clinical Pathology, 1975
- Disorders of Bone Marrow ProductionPediatric Clinics of North America, 1972
- Analytical Review: Spontaneous Chromosomal Breakage and High Incidence of Leukemia in Inherited DiseaseBlood, 1971
- Chromosome Abnormalities in Constitutional Aplastic AnemiaNew England Journal of Medicine, 1966
- Zur Fanconi-Anämie (FA)European Journal of Pediatrics, 1964
- IMPROVEMENTS IN EPOXY RESIN EMBEDDING METHODSThe Journal of cell biology, 1961