How To Prevent Chromosomal Abnormalities In Fetus? | By Dr. Kiran Bakane
Вставка
- Опубліковано 26 сер 2024
- In this video, we will explore the various tests available for detecting chromosomal abnormalities in fetuses, providing detailed information on each procedure and its benefits. From non-invasive prenatal testing (NIPT) to amniocentesis, we will discuss how each test works and its potential implications for the health of the baby. By understanding these tests, expectant parents can make informed decisions to prevent and address chromosomal abnormalities.
------------------------------------------
For Appointment Contact
8287944008
drkiranbakane@gmail.com
Address: Plot no. 35, Pragati, Housing Society, Near Chhatrapati Chowk, Wardha Road Nagpur, 440015
--------------------------------------------------
Tags:-
Dr. Kiran Sri Chittala
genetic screening during pregnancy
chromosomal abnormalities in baby
prenatal genetic testing
fetal chromosomal abnormalities prevention
amniocentesis procedure
non-invasive prenatal testing
chromosomal abnormalities ultrasound
genetic counseling during pregnancy
prenatal screening for genetic disorders
preventing birth defects in fetus
what are the diagnostic procedures for genetic and chromosomal abnormalities
genetic and chromosomal disorders
genetic and chromosomal abnormalities
genetic and chromosomal mutations
genetic and chromosomal testing
genetic and chromosomal anomalies
genes and chromosomes
genetic and chromosomal issues in embryo
prevent chromosomal abnormalities
down syndrome
ivf
downs syndrome
down syndrome baby
how to prevent down syndrome
down syndrome treatment
what is down syndrome
prenatal screening
prenatal testing
prenatal diagnosis
prenatal genetic testing
genetic screening
prenatal screenings
trisomy 21 prenatal screening
prenatal genetic screening
non-invasive prenatal screening
screening
first trimester screening
infertility
genetic and chromosomal abnormalities in fetus
combined first trimester screening
quadruple marker
nipt
chorionic villus sampling
cordocentesis
amniocentesis
who should do the invasive test
high risk in screening test
serological test
when to do this tests
Well said talk,, that’s appreciable
Doctor said us intermediate risk.. What should we do??
Useful info doctor
Some information about trisomy 10
U look more like south indian andhra especially,,, am I right mam?
My wife's NT scan and Double marker reports are low risk. Should we go for NIPT ? Or we can skit NIPT ?
With normal NT scan and double marker low risk and no other genetic problem in the family, NIPT is not recommended.
I got High Risk in NIPT test and doctors said no hopes for this pregnancy also they said 90% is confirmed that baby will have abnormalities so they suggest us to terminate baby
Then wt the decision U too.
I got also high risk in NIPT nd my gync Dr said 99 % baby will hv down syndrome she was suggested to terminate nd we took decision to terminate the baby....nd we did😢😢😢😢I lost my baby boy in 4 months of pregnancy....
Same problem..@@jyotiagrawal5001
@@jyotiagrawal5001 i too lost my baby 😢😢😢
Mam my wife NT is 2.8 mm is it normal 14 weeks
14trisomy detected onicroarray test report of product of conception.
Missed abortion occurred at 15 week..foetal growth restricted at 7week only..my question is what would be future of next pregnancy..what are the chances of reccurnce of this trisomies..is there any one who has experienced same and later on gave birth to healthy child??
Many times these trisomies occur due to cell division during baby formation. Recurrence is less than 1%. But we need to check for parental chromosomal pattern for risk of inheritance in case of multiple miscarriages. Please do contact a geneticist or obstetrician before planning next pregnancy.
क्या आप हिंदी जानते हैं?
Mammm