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Endometrial Ablation Procedure
Treatment of Treatment of Breast Cancer
Management of Abortion
Hormonal Replacement Therapy Treatment
Caesarean Section Procedure
Treatment of Gynae Problems
Gynecology Laparoscopy Procedures
Treatment Of Female Sexual Problems
Treatment Of Menopause Related Issues
Treatment Of Menstrual Problems
Treatment of Mirena (Hormonal Iud)
Pap Smear Procedure
Polycystic Ovary Syndrome Treatment
Treatment of Uterine Bleeding
Antenatal And Postnatal Exercise
My friend is 20 years old and she has done sex before 1 month but condom was used during sex. Her periods are usually delayed by 2-4 days but after sex she has not received the period even after 20 days of her period. She feels the same pain as in period time but not getting with period. Please help.
I have a small lump in my left breast since 2 years. Also a serous discharge is coming out from nipple while pressing. No dimpling and pain. Is it a carcinoma or fibroadenoma? The amount of discharge is hardly one drop. Whether it s a carcinoma? Need a surgery?
Thalassemia is a genetic (which is 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
If you wish to discuss about any specific problem, you can consult a doctor and ask a free question.
I am 6 week pregnant women I have query regarding thyroid when I test TSH on dated 13th sep the result will shows 3.98. As per my gynecologist it is normal but when I go for second opinion then 2nd gynecologist said it is slightly high and you have to take medicine. Now today (dt 18 sep) I again test my TSH and result is different from last result (Today result = 3.237).I am worried about my baby and confused what to do. Please help me out. # I had never suffer from any thyroid before pregnancy.
My wife is pregnant and in 14 weeks she is having high b.p 150/110. Earlier in 2006 she had faced the same problem of high b.p due to which premature baby in seventh month happened of 950 grm .The baby does not survived. In 2009 she given the birth a baby of2. 5 kg in36or 37 weeks which is now 7 year old. But now in 2016 she is having high b.p in 14 weeks. Doc prescribed her gravidol 100 mg thrice daily. Now she is in 17 weeks and her b.p is 130/95. She is also taking ecosprin. Iron. Protein powder. Susten 300. Argiplus powder. I am afraid of her b.p will make us to face same problem that happen in 2006 of severe PIH and IUGR. My wife age is 35. She is also having p.c.os. She is also taking eltroxin 50.
Use a cast iron pan for cooking whenever possible (while using tomato sauces and other acidic and moist foods. I read this somewhere and here I have a doubt, actually everybody says not to cook acidic foods like tomato etc. And moist like gravies of Indian curries (with acidic contact too) in an iron pan. So is this should not be obeyed during pregnancy, or does it have good effects during pregnancy, can you please help me understanding this. Thank you.
An oil massage is one of the best remedies for dry skin. Using an anti-aging oil would be best as it would be highly absorbant.