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Kulekhara, also known as "Kulekhara leaf" or "Kulekhara herb," is traditionally used in some cultures for various health benefits, but there is no scientific evidence to support its effectiveness in curing thalassemia. Thalassemia is a genetic blood disorder that affects hemoglobin production, and its management typically involves blood transfusions, iron chelation therapy, and other medical interventions. It's crucial for individuals with thalassemia to consult healthcare professionals for appropriate treatment rather than relying on herbal remedies.
What else can I help you with?
Is kulekhara leaf simple?
is kulekhara leaf compound
What the English name for bengali word kulekhara leaf?
no
Are there other names for Thalassemia disease?
Alpha thalassemia silent carrierAlpha thalassemia minor, also called alpha thalassemia traitHemoglobin H diseaseAlpha thalassemia major, also called hydrops fetalisBeta thalassemia minor, also called beta thalassemia traitBeta thalassemia intermediaBeta thalassemia major, also called Cooley's anemia or beta-zero (ß0) thalassemiaBeta-plus (ß+) thalassemiaMediterranean anemia
Is thalassemia a type of cancer?
Thalassemia is an autosmal recessive blood disease. That means that it is an inherited disease. Thalassemia in more common in Mediteranian people.
What is classification of Thalassemia?
Thalassemia is classified mainly into two types: alpha thalassemia and beta thalassemia, based on which globin chain is affected. Alpha thalassemia occurs due to mutations in the alpha-globin genes, while beta thalassemia results from mutations in the beta-globin genes. Each type can further be categorized into various subtypes based on the severity of the condition, such as thalassemia minor (trait) and thalassemia major (Cooley's anemia). The classification helps determine the appropriate management and treatment strategies for affected individuals.
What chromosome is thalassemia carried on?
Thalassemia is carried on chromosome 11 and chromosome 16, depending on the type. The alpha-thalassemia gene is located on chromosome 16, while the beta-thalassemia gene is found on chromosome 11. Mutations in these genes affect the production of hemoglobin, leading to the various forms of thalassemia.
Can minor thalassemia carrier and alpha marry?
Yes, A "carrier" of alpha thalassemia and of beta thalassemia can marry, but not to someone with any hemoglobinopathy. Prof. Kornfeld Pal
Can mild thalassemia be a major thalassemia?
No. A minor form of the blood disorder thalassemia is when you inherited just one beta thalassemia gene, along with a normal beta-chain gene. This manifests as mild anaemia with a slight lowering of the hemoglobin level in the blood. No treatment is require. By contrast, a thalassemia major, also known as Cooley's Disease, is when one is born with two genes for beta thalassemia and no normal beta-chain gene. This is a serious disorder.
What is alfa-thalassamie?
Anemia These drugs include epoetin Alfa (Procrit, Epogen, and Eprex) and darbepoetin Alfa (Aranesp).... The two major forms are thalassemia minor and thalassemia major (Cooley's anemia, beta thalassemia).....What Is Thalassemia?(also known as Mediterranean anemia, or Cooley's Anemia) is a genetic blood disease. People born with this disease cannot make normal hemoglobin (anemia) which is needed to produce healthy red blood cells.Who carries Thalassemia?People of Chinese, South Asian, Middle Eastern, Mediterranean or African origin.What is Thalassemia Minor?People with a thalassemia mutation only in one gene are known as carriers or are said to have thalassemia minor. Thalassemia minor results in no anemia or very slight anemia. People who are carriers do not require blood transfusion or iron therapy, unless proven to be iron deficient.What is Thalassemia Major?Children born with thalassemia major usually develop the symptons of severe anemia within the first year of life. Lacking the ability to produce normal adult hemoglobin, children with thalassemia major:- are chronically fatiqued- fail to thrive, and- do not grow normallyProlonged anemia will cause bone deformities and eventually will lead to death within the first decade of life. The only treatment to combat severe anemia is regular blood transfusions.How can Thalassemia be treated?Regular blood transfusions allow patients with thalassemia major to grow normally and be active. Unfortunately, transfusions result in deadly accumulation of iron in the hearts and livers of patients by their teenage years. If the excess iron is not removed then the patients may suffer from a premature death due to iron overload.Nowadays, drugs designed to remove excess iron (iron chelators) have significantly changed the prognosis of thalassemia major. Patients can grow and develop normally, with relatively normal heart and liver functions. Adult patients are living into their forties and some have children of their own.Despite improved prognosis, many patients find the nightly 10 hour infusions difficult or painful and are reluctant to comply with their doctor's orders. These patients are not free of risk and may die prematurely due to iron overload.Current treatments allow thalassemia patients to live relatively normal lives, however, a cure remains to be found. The genetic cause of thalassemia was one of the first genes discovered in the 1970's, yet 30 years later, gene therapy still eludes thalassemia patients.Do you carry Thalassemia?Many people from the areas of the world where thalassemia is common carry the gene for it on one chromosome (that is, they have thalassemia minor). You may believe that your blood has been tested for this specific gene but testing for thalassemia requires a special blood test. To be tested your doctor must order a blood test called HEMOGLOBIN ELECTROPHORESIS which can identify a carrier of thalassemia.If you, your parents or ancestors are from an area of the world where thalassemia is common, PLEASE REQUEST hemoglobin electrophoresis blood test from your doctor.It is important to identify yourself as a possible carrier of thalassemia (thalassemia minor). A person with thalassemia minor has a 25%(1 in 4) chance of having a baby with THALASSEMIA MAJOR if his/her mate also has thalassemia minor. http://www.thalassemia.ca/viewarticle.asp?aID=31&searchQ=F.A.Q
I am a thalassemia patient.i have to transfuse blood regulerly and im doin very well..my bf is goin to check for thalassemia...if he is a thala carrier and if we marry will we have a child like me?
If you have Thalassemia major but your boyfriend is not a carrier then the child will be born a healthy carrier (thalassemia minor) but shouldn't need blood transfusions. If your boyfriend is a carrier then you would have a 50% chance of having a child with thalassemia major like you do.
Is thalassemia hereditary?
yes
How long a human survive with thalassemia and with the recessive genes?
Those with thalassemia can expect to live until they are 50 or more.
