Alpha Thalassemia Alpha ThalassemiaRelated Procedures & Tests « Back to Alpha Thalassemia Index Sorted Alphabetically A-Z Sort by popularity Amniocentesis Blood Transfusion Bone Marrow Aspiration and Biopsy Complete Blood Count (CBC) Hemoglobin Sorted by Popularity (as on MedicineNet) Sort alphabetically Hemoglobin Complete Blood Count (CBC) Blood Transfusion Bone Marrow Aspiration and Biopsy Amniocentesis Suggested Reading on Alpha Thalassemia by Our Doctors Related Diseases & Conditions 18 articles Anemia Anemia is the condition of having less than the normal number of red blood cells or less than the normal quantity of hemoglobin in the blood. The oxygen-carrying Arrhythmia An arrhythmia is an abnormal heart rhythm. With an arrhythmia, the heartbeats may be irregular or too slow (bradycardia), to rapid (tachycardia), or too Gallstones Gallstones are stones that form when substances in the bile harden. Gallstones (formed in the gallbladder) can be as small as a grain of sand or as large Jaundice (Adults) Jaundice in adults may be caused by a variety of medical diseases or conditions. Some cases of jaundice can be managed at home with a doctor's supervision, Heart Attack Heart attack happens when a blood clot completely obstructs a coronary artery supplying blood to the heart muscle. A heart attack can cause chest pain, Puberty The time when boys and girls begin the process of sexual maturation is called puberty. During this time, both sexes undergo a series of biological changes Abnormal Heart Rhythms (Heart Rhythm Disorders) Heart rhythm disorders vary from minor palpitations, premature atrial contractions (PACs), premature ventricular contractions (PVCs), sinus tachycardia, Sickle Cell Disease (Sickle Cell Anemia) Sickle cell anemia (sickle cell disease), a blood disease which shortens life expectancy, is cause by an inherited abnormal hemoglobin. Symptoms may include Beta Thalassemia Beta Thalassemia is the most familiar type of thalassemia. Thalassemia is not just one disease but rather a complex series of genetic (inherited) disorders G6PD Deficiency G6PD deficiency (Glucose 6-phosphate dehydrogenase) leads to a condition called hemolytic anemia. Causes of G6PD deficiency is an abnormal gene located Enlarged Spleen (Splenomegaly) An enlarged spleen or splenomegaly is generally caused by other diseases or conditions such as infections, cancers, blood disorders, or decreased blood Heart Failure Heart failure is caused by many conditions including coronary artery disease, heart attack, cardiomyopathy, and conditions that overwork the heart. Symptoms Heart Disease (Coronary Artery Disease) Heart disease (coronary artery disease) occurs when plaque builds up in the coronary arteries, the vessels that supply blood to the heart. Heart disease Genetic Disease Genetic disease is a disorder or condition caused by abnormalities in a person's genome. Types of genetic inheritance include single inheritance (for example, Malaria Malaria is a disease that is spread by the bite of an infected Anopheles mosquito. Malaria symptoms include fever, chills, nausea, vomiting, and body aches. Genetic Counseling Your health care provider may refer you to a genetic professional. Universities and medical centers also often have affiliated genetic professionals, or Pregnancy Planning Pregnancy planning is important to help prevent exposure of the mother and fetus to potentially harmful medications and substances during the early days, Newborn Jaundice (Neonatal Jaundice) Newborn jaundice or neonatal jaundice is a yellowish discoloration of the mucous membranes, whites of the eyes, and skin of a newborn. Newborn jaundice Medications 3 articles Procedures & Tests 5 articles Pictures, Images & Quizzes 0 articles Doctor's & Expert's Views 0 articles Health News 0 articles Health Features 1 articles STAY INFORMED Get the latest health and medical information delivered direct to your inbox!