Hemoglobin h disease
Thalassemias are inherited blood disorders. If you have one, your body makes fewer healthy red blood cells and less hemoglobin. Hemoglobin is a protein that carries oxygen to the body. That leads to anemia. Thalassemias occur most often among people of Italian, Greek, Middle Eastern, Southern Asian, and African descent.Thalassemias can be mild or severe. Some people have no symptoms or mild anemia. The most common severe type in the United States is called Cooley's anemia. It usually appears during the first two years of life. People with it may have severe anemia, slowed growth and delayed puberty, and problems with the spleen, liver, heart, or bones.Doctors diagnose thalassemias using blood tests. Treatments include blood transfusions and treatment to remove excess iron from the body. If you have mild symptoms or no symptoms, you may not need treatment. In some severe cases, you may need a bone marrow transplant.NIH: National Heart, Lung, and Blood Institute
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Top doctors who continously share their opinions on Hemoglobin h diseaseAttached To Charitable Organizations As Honorary Holistic Health Consultant
HOLISTIC HEALTH CONSULTANT PRACTISING COMPLEMENTARY& INTEGERATED MEDICINE Especially EBH..Evidence Based HOMOEOPATHY Since 1984 *****************************************************A Ph.D Thesis Guide & Assessor
M.D..FF.HOM, D.A.c..D.Sc.

S.A.S.Hi-Tech Hospital Bhopal
Rmo

Super Specialist in Reproductive Endocrinology

Phansidewa BPHC
Additional Medical Officer
Darjeeling ICMS, Calcutta National Medical College
Dip CMS, Condensed Medical Course


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