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| | Johns Hopkins University: Hematology eDigest |
 | | To be fair, while sickle cell anemia is a monogenic disorder, its clinical phenotype is distinctly multifarious due in part to the epistatic effects of concomitantly inherited linked and unlinked genes, and in part, to the multi-organ damage inflicted on the host by the sickling process. |
 | | Furthermore, it is important to acknowledge the progressive increase in longevity of patients with this disorder, owing to effective immunization, infection control, and the recognition and prompt treatment of complications such as the acute chest syndrome. |
 | | Extended phenotype matching has the benefit of preventing alloimmunization and its attendant morbidity, mortality and hospital costs. |
| www.hopkinscme.net /ofp/hematologyedigest/newsletter/detail_063005.htm (2449 words) |
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