Rubella Virus Treatment
Hello sir, my age is 26 and wife is 22 years old and me and my wife had sex many times before after that my wife gets pe ...
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Better use condom for the time being and follow up with a doctor for regular check up of your wife. Good luck.
45 year male. Last week of august 2019 did oral sex (kissed lips and sucked the vagina) without any protection n also va ...
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You have done tests like mad, it's hiv phobia, part of ocd. It will be much better if you can please take private consult with audio video chat and then I can guide you properly and explain you what is to be done. Ideally you need a good personal consultation and rounds of counseling. Take care. Don't fo any more tests.
My baby died in the womb with the rubella virus in the 8th month of pregnancy. The doctor said this virus is not active ...
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It can be detected by the blood test. You should think of taking proper treatment. You can consult me at Lybrate for homoeopathic treatment.
Namaskar doctor. This query is about my younger sister. She is married. It is her two years of marriage. Before one year ...
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It’s best to get vaccinated against rubella before you get pregnant to protect your baby. You should wait at least 4 weeks after getting the vaccine to become pregnant. If you’re already pregnant, you shouldn’t get the vaccine.
Hi, What are symptoms of rubella virus? I want to know please describe in detail? Treatment and prognosis? ...
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Mild fever, sore throat, typical lesion on soft palate, rashes on body, may be associated other complaints like earache, lymph nodes enlarged in some case. No specific treatment- depends on symptoms Few get secondary complication like infection, majority sail through well more so in children. During pregnancy more complications. Can be prevented by earlier vaccination
What cause abnormal babies development in mother womb and in which month it can be known during pregnancy. ...
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An estimated 303 000 newborns die within 4 weeks of birth every year, worldwide, due to congenital anomalies. Congenital anomalies can contribute to long-term disability, which may have significant impacts on individuals, families, health-care systems, and societies. The most common, severe congenital anomalies are heart defects, neural tube defects and Down syndrome. Although congenital anomalies may be the result of one or more genetic, infectious, nutritional or environmental factors, it is often difficult to identify the exact causes. Some congenital anomalies can be prevented. Vaccination, adequate intake of folic acid or iodine through fortification of staple foods or supplementation, and adequate antenatal care are just 3 examples of prevention methods. Causes and risk factors Although approximately 50% of all congenital anomalies cannot be linked to a specific cause, there are some known genetic, environmental and other causes or risk factors. Genetic factors Genes play an important role in many congenital anomalies. This might be through inherited genes that code for an anomaly, or resulting from sudden changes in genes known as mutations. Consanguinity (when parents are related by blood) also increases the prevalence of rare genetic congenital anomalies and nearly doubles the risk for neonatal and childhood death, intellectual disability and other anomalies. Some ethnic communities (such as Ashkenazi Jews or Finns) have a comparatively high prevalence of rare genetic mutations such as Cystic Fibrosis and Haemophilia C. Socioeconomic and demographic factors Low-income may be an indirect determinant of congenital anomalies, with a higher frequency among resource-constrained families and countries. It is estimated that about 94% of severe congenital anomalies occur in low- and middle-income countries. An indirect determinant, this higher risk relates to a possible lack of access to sufficient, nutritious foods by pregnant women, an increased exposure to agents or factors such as infection and alcohol, or poorer access to healthcare and screening. Factors often associated with lower-income may induce or increase the incidence of abnormal prenatal development. Maternal age is also a risk factor for abnormal intrauterine fetal development. Advanced maternal age increases the risk of chromosomal abnormalities, including Down syndrome. Environmental factors Maternal exposure to certain pesticides and other chemicals, as well as certain medications, alcohol, tobacco and radiation during pregnancy, may increase the risk of having a fetus or neonate affected by congenital anomalies. Working or living near, or in, waste sites, smelters or mines may also be a risk factor, particularly if the mother is exposed to other environmental risk factors or nutritional deficiencies. Infections Maternal infections such as syphilis and rubella are a significant cause of congenital anomalies in low- and middle-income countries. More recently, the effect of in utero exposure to Zika virus on the developing fetus has been reported. In 2015, Brazil detected cases of Zika virus and a spatio-temporally associated increase in microcephaly. By 2016, Brazil reported that of 4180 suspected cases of microcephaly, 270 were confirmed, 462 were discarded and 3448 are still under investigation. This is compared to an average of 163 microcephaly cases recorded nationwide per year. With 6 of the 270 confirmed cases of microcephaly showing evidence of Zika infection, health authorities and agencies are investigating and conducting comprehensive research to confirm a causal link. Following the Zika outbreak in French Polynesia, health authorities reported an unusual increase in the number of congenital malformations in babies born between March 2014 and May 2015. Maternal nutritional status Maternal folate insufficiency increases the risk of having a baby with a neural tube defect while excessive vitamin A intake may affect the normal development of an embryo or fetus. Detection Health care before and around the time of conception (preconception and peri-conception) includes basic reproductive health practices, as well as medical genetic screening and counselling. Screening can be conducted during the 3 periods listed: Preconception screening can be useful to identify those at risk for specific disorders or at risk of passing a disorder onto their children. Screening includes obtaining family histories and carrier screening, and is particularly valuable in countries where consanguineous marriage is common. Peri-conception screening: maternal characteristics may increase risk, and screening results should be used to offer appropriate care, according to risk. This may include screening for young or advanced maternal age, as well as screening for use of alcohol, tobacco or other risks. Ultrasound can be used to screen for Down syndrome and major structural abnormalities during the first trimester, and for severe fetal anomalies during the second trimester. Maternal blood can be screened for placental markers to aid in prediction of risk of chromosomal abnormalities or neural tube defects, or for free fetal DNA to screen for many chromosomal abnormalities. Diagnostic tests such as chorionic villus sampling and amniocentesis can be used to diagnose chromosomal abnormalities and infections in women at high risk. Neonatal screening includes clinical examination and screening for disorders of the blood, metabolism and hormone production. Screening for deafness and heart defects, as well as early detection of congenital anomalies, can facilitate life-saving treatments and prevent progression towards some physical, intellectual, visual, or auditory disabilities. In some countries, babies are routinely screened for abnormalities of the thyroid or adrenal glands before discharge from the maternity unit.
Hello doctor. Rubella kitne time m thik hota h or ye thik hone ke baad dubara to nhi ho jata na or rubella virus thik ho ...
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Ji thik ho jata he.. Aur Uske 6 months bad conceive kare... Homoeopathic treatment bhi Suru kare Sath Sarah for healthy pregnancy..
Hello Doctor, I’ve taken torch test in my report Anti Toxoplasma says nonreactive but shows the reading (0.06) normal ra ...
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It does not cause problem to conceive but the child may be born with congenital anomalies. It is advised that you get treated for these infections before deciding to bear a child. Your report of Rubella indicates either you have been exposed to the virus or you have been vaccinated and therefore are immune against the virus. Rubella is often spread through coughing or sneezing. It can also be transmitted when people put their fingers in their mouth or nose after touching an infected surface. CMV is passed from person to person through close contact with body fluids, such as saliva, semen, vaginal fluids, blood, urine, tears and breast milk. You can get CMV when you touch these fluids with your hands and then touch your eyes, nose or mouth, which are mucous membranes. A positive test for CMV IgG indicates that a person was infected with CMV at some time during their life, but does not indicate when a person was infected. This means that you have got the infection from your partner or could spread it to your partner if you are actually infected with it.
Gone through last year of 8 month baby girl and than Dr. gave a rubella vaccination igg activated three months after. Fe ...
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in torch profile which inf is showing igM +ve as there are very few chances that u again get Rubella igM +ve .thereare other viruses also which may be igm +ve so u need to get treatment for that .rubella will not help u
Sir my wife had an abortion a year ago after that she had done torch test results rubella igg 99.9 IU/ml cytomegalovirus ...
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TORCH IgG values in positive range indicate past infection. If IgM values are negative, there is no current infection, and does not require any treatment. There could be several other reasons for not getting pregnant. To check for fallopian tube patency, get Hysterosalpingography done on Day 9 of menses. Fallopian tube blockage needs to be treated by surgery, laparoscopic preferably.
