Doctor in Patna Hematolgy Clinic
Treatment of Anemia
Treatment of Blood Cancer
Treatment of Low Platelets
Treatment of Thalassemia
Treatment of Lymphoma
Treatment of Thrombotic Thrombocytopenic Purpura
Treatment of Leukemia
Treatment of Hemophilia
Treatment of Multiple Myeloma
Treatment of Hodgkin lymphoma
Blood Disorders Treatment
Treatment of Sickle Cell Anemia
Treatment of Thrombocytopenia
Treatment Of Aplastic Anemia
Stem Cell Transplant
Treatment of Polycythemia Vera
Treatment of Bleeding disorder
Treatment of Methemoglobinemia
Treatment of Blood Disorders
Treatment of Hemolytic Anemia
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Sudhansu Bhusan Nanda
I found the answers provided by the Dr. Avinash Singh to be very helpful and saved my life. thanking 7..pls suggest near future best physician to consult ear to my locality..
Doctor was unavailable.And even no email regarding cancellation of appointment was sent to me. This caused me a lot of inconvenience
Cancer is the most dangerous and harmful disease of the world, which has various reasons to affect the body in any stage of life. This is also the good thing to know that there are a lot of treatments available in the medicine arena which can completely or partially treat cancer. But the individual and the family members of them need to be confident enough with the treatment and expertise of the doctor. Blood Cancer is a life taking disease and the treatment for it is must. The medicines should be start recovery from any age of the sufferer and stage of the disease. The treatment will have some side effects and fast to react to symptoms and should be affordable as well.
As said before that the symptoms of different types of the cancer vary but some general symptoms are there which are found in most of the cancer patients.
Haematology is less known, but a very important branch of medical science. This branch is concerned with the study of blood, blood diseases and the blood-forming organs as well. Treatment based on the Haematology for blood cancer can be quite successful as compared to general remedies. The modern Haematology made cancer easy to cure, comfortable and side effect less. This cost effective method of cancer cure give relief in lesser time and assures the improved quality of life as well. That is the reason that people around the world trust on treatment based upon Haematology because the treatment has all the basic qualities that made it the best cure for cancer.
Thalassemia is a genetic (i.e., passed from parents to children through genes) blood disorder. People with Thalassemia disease are not able to make enough hemoglobin, which causes severe anemia. Hemoglobin is found in red blood cells and carries oxygen to all parts of the body. When there is not enough hemoglobin in the red blood cells, oxygen cannot get to all parts of the body. Organs then become starved for oxygen and are unable to function properly.
There are two types of Thalassemia disease-
- Alpha Thalassemia disease: There are two main types of Alpha Thalassemia disease. Alpha Thalassemia Major is a very serious disease in which severe anemia begins even before birth. Pregnant women carrying affected fetuses are themselves at risk for serious pregnancy and delivery complications. Another type of Alpha Thalassemia is Hemoglobin H disease. There are varying degrees of Hemoglobin H disease.
- Beta Thalassemia disease: Beta Thalassemia Major (also called Cooley's Anemia) is a serious illness. Symptoms appear in the first two years of life and include paleness of the skin, poor appetite, irritability, and failure to grow. Proper treatment includes routine blood transfusions and other therapies.
Causes of Thalassemia-
Thalassemia occurs when there’s an abnormality or mutation in one of the genes involved in hemoglobin production. You inherit this genetic defect from your parents.
If only one of the parents is a carrier for thalassemia, the child may develop a form of the disease known as thalassemia minor. If this occurs, the born child probably won’t have symptoms, but he/she will be a carrier of the disease. Some people with thalassemia minor do develop minor symptoms.
If both of your parents are carriers of thalassemia, you have a greater chance of inheriting a more serious form of the disease.
The symptoms depend on the type of thalassemia:
- Thalassemia Minor: Thalassemia minor usually doesn’t cause any symptoms. If it does, it causes minor anemia.
- Beta-thalassemia: Beta-thalassemia comes in two serious types, which are thalassemia major, or Cooley’s anemia, and thalassemia intermedia. The symptoms of thalassemia major generally appear before a child’s second birthday. The severe anemia related to this condition can be life-threatening. Other signs and symptoms include:
- frequent infections
- a poor appetite
- failure to thrive
- jaundice, which is a yellowing of the skin or the whites of the eyes
- enlarged organs
This form of thalassemia is usually so severe that it requires regular blood transfusions.
- Alpha-thalassemia: Alpha-thalassemia also has two serious types, which are hemoglobin H disease and hydrops fetalis. Hemoglobin H disease can cause bone issues. The cheeks, forehead, and jaw may all overgrow. Hemoglobin H disease can cause:
- jaundice, which is a yellowing of the skin or the whites of the eyes
- an extremely enlarged spleen
Hydrops fetalis is an extremely severe form of thalassemia. It occurs before birth. Most individuals with this condition are either stillborn or die shortly after being born.
How is thalassemia diagnosed?
Thalassaemia is often detected during pregnancy or soon after birth.
- Screening during pregnancy: Screening to check if a baby is at risk of being born with thalassemia is offered to all pregnant women.
- Testing after birth or later in life: Newborn babies aren't routinely tested for thalassemia because the test used isn't always reliable soon after birth and the condition isn't immediately dangerous. However, the main form of the condition – beta thalassemia major – is often picked up as part of the newborn blood spot test (heel prick). A blood test can be carried out at any point to diagnose the condition if a child or adult has symptoms of thalassemia and the condition wasn't picked up earlier on.
- Testing for the Thalassemia Trait- A blood test can be done at any time to find out if you have the thalassemia trait and are at risk of having a child with the condition. This can be particularly useful if you have a family history of the condition or your partner is known to carry thalassemia.
If your child has thalassemia, blood tests may reveal:
- A low level of red blood cells
- Smaller than expected red blood cells
- Pale red blood cells
- Red blood cells that are varied in size and shape
- Red blood cells with uneven hemoglobin distribution, which gives the cells a bull's-eye appearance under the microscope
Blood tests may also be used to:
- Measure the amount of iron in your child's blood
- Evaluate his or her hemoglobin
- Perform DNA analysis to diagnose thalassemia or to determine if a person is carrying mutated hemoglobin genes
Treatment for Thalassemia-
The treatment for thalassemia depends on the type and severity of disease involved. Your doctor will give you a course of treatment that will work best for your particular case.
Some of the utilized treatments include:
- blood transfusions
- a bone marrow transplant (BMT)
- medications and supplements
- possible surgery to remove the spleen or gallbladder
In case you have a concern or query you can always consult an expert & get answers to your questions!
Anemia (or anaemia) is a medical condition which generally occurs in a human body because of the lack of required healthy red blood cells (RBCs) or hemoglobin in the blood. Diagnosis of anemia is done through a blood test, a man is anemic when his hemoglobin level is less than 13.5 gram/100 ml and a woman is anemic when her hemoglobin level is less than 12.0 gram/100 ml.
Risk factors: People suffering from long-term or chronic diseases such as cancer are more susceptible of developing anemia. Hemoglobin is the salient constituent of red blood cells and is an iron rich protein. It provides the red color to the blood and binds oxygen. Red blood cells carry this oxygen to all the vital tissues and organs of the body. Due to lack of appropriate amount of red blood cells, the amount of blood required in a body to function normally is also low. One of the most prominent causes of occurrence of anemia is the deficiency of required amount of nutritional iron, vitamin B-12, and folate in the body. This iron is needed for the formation of hemoglobin. Apart from these causes, the other causes of anemia comprise of the following:
- Loss of blood
- Insufficient production of red blood cells (inadequate intake of iron, vitamin B-12)
- Fast rate of destruction of red blood cells (disorders of liver and hemorrhage)
Diagnosis: It is relatively easy to detect an anemic person. The symptoms of anemia include pale appearance, complaint of cold, giddiness, unsteadiness, laziness, particularly when the person is in action or is standing up. Sometimes people suffering from anemia crave for eating clay, ice, or even dirt. Also, there are complains of exhaustion along with issues of constipation and concentration. Other indications of anemia are brittle nails, gasps for breath even in mild activities, and pain in the chest. Since the level of oxygen in the blood is low, there could be even scope of a heart attack.
A person suffering from anemia is usually diagnosed on the basis of a complete blood count. The blood test brings out if serum folate levels are quite low. In case the anemia is severe, sometimes doctors take the help of erythropoietin injections so as to foster the production of red blood cells in the bone marrow. In case there is bleeding or if the level of hemoglobin is low, it might become essential to carry out blood transfusion.
Treatment: Anemia is straightforward to diagnose and treat, but at the same time could prove to be deadly if it is left undiagnosed. Proper heed should be paid to the intake of adequate and required food which is rich in vitamins and minerals, dietary iron, folic acid, including other vitamins and minerals.
Haematology is a science, which studies the functioning of blood, blood producing organs and blood related diseases. Previously people are not aware of the functioning of Haematology and its effectiveness. But as more and more research is beign conducted on this health care science the modern world is introduced with this amazing stream of medical science.
Haematology can study and provide best curing measures for many severe diseases and one of the diseases, which are considered as the most dangerous is Thrombocytopenia. This is the condition in which the blood cell fragments known as platelets reduce. Difficulty faced by the body to clot the blood and stop the bleeding is a major symptom and when the platelet count reduces too much then mild to severe bleeding happens. Bleeding can be inside the body, on the surface of the body or underneath the skin as well.
How to control it?
The individuals suffering from lack of platelet count or Thrombocytopenia are advised some preventive measures to maintain the conditions from becoming severe.
- People should avoid the medicine that they know had decreased the platelet in the past.
- They should avoid alcohol consumption which slows down the production of platelets.
- Avoid contact with toxic chemicals like arsenic, pesticides or benzene as they can slow down the production of platelets.
- Be aware of the substances or medicines that may affect the counts of platelets or increases the risk of bleeding.
Haematology is very helpful for doctors to know the hidden causes of blood related diseases. To cure the low platelet count many effective medicines are available in the various health care systems. There are many Haematology experts who are accomplished with their expertise in treating people. Patients of blood cancer should see the best doctor and get the best remedies to live a happy and pain free life. In case you have a concern or query you can always consult an expert & get answers to your questions!