Cancer Center Virtual Tour

Hemoglobin C disease - Overview

Alternative Names

Clinical hemoglobin C

Definition of Hemoglobin C disease:

Hemoglobin C disease is a blood disorder passed down through families. It leads to a type of anemia, which causes red blood cells to break down earlier than normal.

Causes, incidence, and risk factors:

Hemoglobin C is a problem with hemoglobin, the part of red blood cells that carry oxygen. It is a type of hemoglobinopathy. The disease is caused by problem with a gene called beta globin.

The disease most often occurs in African Americans. You are more likely to develop hemoglobin C disease if someone in your family has had it.

Blood cells

Reviewed last on: 11/14/2008
David C. Dugdale, III, MD, Professor of Medicine, Division of General Medicine, Department of Medicine, University of Washington School of Medicine; and James R. Mason, MD, Oncologist, Director, Blood and Marrow Transplantation Program and Stem Cell Processing Lab, Scripps Clinic, Torrey Pines, California. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.

References

Goldman L, Ausiello D. Cecil Textbook of Medicine. 23rd. Philadelphia, Pa: WB Saunders; 2007:1225-1226.

The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. © 1997- A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.

Home > Medical Reference > Encyclopedia (English)