The natural history of sickle cell disease
- PMID: 23813607
- PMCID: PMC3784812
- DOI: 10.1101/cshperspect.a011783
The natural history of sickle cell disease
Abstract
The term sickle cell disease embraces a group of genetic conditions in which pathology results from the inheritance of the sickle cell gene either homozygously or as a double heterozygote with another interacting gene. The spectrum of resulting conditions is therefore influenced by the geography of individual hemoglobin genes, but in most populations, the commonest genotype at birth is homozygous sickle cell (SS) disease. Because this genotype generally manifests a greater mortality, the relative proportion of sickle cell genotypes is influenced by age as well as the geographical distribution of individual genes.
References
-
- Adams RJ, McKie VC, Hsu L, Files B, Vichinsky E, Pegelow C, Abboud M, Gallagher D, Kutlar A, Nichols FT, et al. 1998. Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography. N Engl J Med 339: 5–11 - PubMed
-
- Al Arrayed S 2005. Campaign to control genetic blood diseases in Bahrain. Community Genet 8: 52–55 - PubMed
-
- Bakanay SM, Dainer E, Clair B, Adekile A, Daitch L, Wells L, Holley L, Smith D, Kutlar A 2005. Mortality in sickle cell patients on hydroxyurea therapy. Blood 105: 545–547 - PubMed
-
- Balkaran B, Char G, Morris JS, Serjeant BE, Serjeant GR 1992. Stroke in a cohort study of patients with homozygous sickle cell disease. J Pediatr 120: 360–366 - PubMed
-
- Baum KF, Dunn DT, Maude GH, Serjeant GR 1987. The painful crisis of homozygous sickle cell disease: A study of risk factors. Arch Int Med 147: 1231–1234 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical