2011 Group Project 1
From Embryology
Note - This page is an undergraduate science embryology student group project 2011. |
Thalassemia
Introduction
- a syndrome derived from the thalassa (sea) and haima (blood)
- a group of hereditary blood disorders
- reduced or absent beta globin chain synthesis caused by mutations, resulting in reduced Hb in red blood cells (RBC), decreased RBC production and anemia.
- Most thalassemias are inherited as recessive traits.
History
Epidemiology
Etiology
Clinical manifestations
Diagnostic Procedures
Treatment
Current/future research possibilities
Glossary
References
2011 Projects: Turner Syndrome | DiGeorge Syndrome | Klinefelter's Syndrome | Huntington's Disease | Fragile X Syndrome | Tetralogy of Fallot | Angelman Syndrome | Friedreich's Ataxia | Williams-Beuren Syndrome | Duchenne Muscular Dystrolphy | Cleft Palate and Lip