Hemoglobin C disease is a blood disorder passed down through families. It leads to a type of anemia, which occurs when red blood cells break down earlier than normal.
Alternative NamesClinical hemoglobin C
Causes, incidence, and risk factorsHemoglobin C is an abnormal type of hemoglobin, the protein in red blood cells that carries 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 have hemoglobin C disease if someone in your family has had it.
SymptomsMost people do not have symptoms. Occasionally, jaundice may occur. Some persons with this disease may develop gallstones that require treatment.
Signs and testsPhysical examination may show an enlarged spleen.
Tests that may be done include:
Usually no treatment is needed. Folic acid supplementation may help your body produce normal red blood cells and improve the symptoms of the anemia.
Expectations (prognosis)People with hemoglobin C disease can expect to lead a normal life.
ComplicationsComplications include anemia, gall bladder disease, and enlargement of the spleen.
Calling your health care providerCall your health care provider if you have symptoms of hemoglobin C disease.
PreventionGenetic counseling may be appropriate for high-risk couples who wish to have a baby.
ReferencesSteinberg MH. Sickle cell disease and associated hemoglobinopathies. In: Goldman L, Ausiello D, eds. Cecil Medicine. 23rd ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 167.
Hemoglobin C disease is a blood disorder passed down through families. It leads to a type of anemia, which occurs when red blood cells break down earlier than normal.
Alternative NamesClinical hemoglobin C
Causes, incidence, and risk factorsHemoglobin C is an abnormal type of hemoglobin, the protein in red blood cells that carries 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 have hemoglobin C disease if someone in your family has had it.
SymptomsMost people do not have symptoms. Occasionally, jaundice may occur. Some persons with this disease may develop gallstones that require treatment.
Signs and testsPhysical examination may show an enlarged spleen.
Tests that may be done include:
Usually no treatment is needed. Folic acid supplementation may help your body produce normal red blood cells and improve the symptoms of the anemia.
Expectations (prognosis)People with hemoglobin C disease can expect to lead a normal life.
ComplicationsComplications include anemia, gall bladder disease, and enlargement of the spleen.
Calling your health care providerCall your health care provider if you have symptoms of hemoglobin C disease.
PreventionGenetic counseling may be appropriate for high-risk couples who wish to have a baby.
ReferencesSteinberg MH. Sickle cell disease and associated hemoglobinopathies. In: Goldman L, Schafer AI, eds. Cecil Medicine. 24th ed. Philadelphia, Pa: Saunders Elsevier; 2011:chap 166.
Reviewed ByReview Date: 02/08/2012
Todd Gersten, MD, Hematology/Oncology, Palm Beach Cancer Institute, West Palm Beach, FL. Review provided by VeriMed Healthcare Network; Linda J. Vorvick, MD, Medical Director and Director of Didactic Curriculum, MEDEX Northwest Division of Physician Assistant Studies, Department of Family Medicine, UW Medicine, School of Medicine, University of Washington. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.
Sickle cell anemia.
It is known as a NON-INFECTIOUS disease. as it is caused by the lack of Vitamin C in the body.
Carl Wunderlich discovered that fever is not a disease, but the body's response to a disease. Carl Reinhold August Wunderlich (1815-1877) was a German physician, pioneer psychiatrist, and medical professor. He is known for his measurement of mean healthy human body temperature of 37°C (98.6°F), now known more accurately to be about 36.8°C (98.2°F).
scurvy
c. low HDL and high LDL
Hemoglobin contain C, H, O, N, Fe.
Hemoglobin is a protein in red blood cells that carries oxygen from the respiratory organs to the rest of the body by way of the blood. When someone is lacking in hemoglobin, the condition is known as anemia. Iron is an important vitamin for hemoglobin production, as it increases resistance to stress and disease and improves blood quality. Vitamin C supports the absorption of iron, so it is also necessary to have enough vitamin C for healthy blood.
a and c
DefinitionHemoglobinopathy is a group of disorders passed down through families (inherited) in which there is abnormal production or structure of the hemoglobin molecule.Such disorders include hemoglobin C disease, hemoglobin S-C disease, sickle cell anemia, and various types of thalassemia.ReferencesGolan DE. Hemolytic anemias: red cell membrane and metabolic defects. In: Goldman L, Ausiello D, eds. Cecil Medicine. 23rd ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 165.
Abnormal hemoglobin in your blood cells. Hemoglobin is a protein in the blood cells that allows the cells to carry oxygen and gives them their red color. The abnormal hemoglobin causes the cells to turn from their usual donut shape to a C or sickle shape.
Hemoglobin is on RBCs, not WBCs. Hemoglobin picks up CO2 from cells and takes it to the lungs, where it releases CO2 and picks up O2. Anemia can reduce available Hgb in the bloodstream. So can any illness, condition, or disease which affects RBC production.
liver disease
the mineral is iron.
The Answer is no But if on treatment as I am at the moment then yes the treatment can lower hemoglobin levels and I would like to add that this and all other symptoms are closely monitored by the medical team
Hemoglobin A1 c
C. jeuni is the subtype that most often causes gastrointestinal disease.
C. fetus produces disease outside the intestine, particularly in those with altered immune systems, such as people with AIDS, cancer, and liver disease.