21 - Fetal karyotype ... Down syndrome is a chromosomal abnormality of trisomy 21 . It can be screened using Serum alpha feto protein and Ultrasound . But the confirmation test is done by chromosomal analysis (Karyotype). Amniotic Fluid Index is used to detect poly/ oligohydramnios ...
D serum alpha fetoprotein sir In antenatal period basic screening is msafp then there is increase only they go for fetal karotype sample from chronic villus
ANS -21 - C There are two tests for prenatal screening and determinate test. By usg we check some sign of foetus like down syndrome but its not confirm by this AFI is also check by the usg Serum alpha fetoprotein is produced by foetus but its also a screening test But we know that down syndrome is trisomy of 21th chromosome so karyotype is diagnostic of determination in this we confirm by check the chromosome of foetus.
Ans is D. Alpha feto protein... Triplet test is done around 15-18 weeks to rule out out down's syndrome it includes alpha feto protein, beta hcg and estriol
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21) Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients. H Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21) Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients. H Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
Fetal karyotyping In this the cells of the fetus collected from in utero and analyse by genetic testing for any extra chromosome in 21 This is usually demonstrates the child with down syndrome
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21) Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients. H Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21) Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients. H Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21) Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients. H Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21) Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients. H Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
@@nursing7863 Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21) Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients. H Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21) Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients. H Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21) Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients. H Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
A good beginning for NIMHANS exam session ...Thank you so much Sir ...
21 - Fetal karyotype ... Down syndrome is a chromosomal abnormality of trisomy 21 . It can be screened using Serum alpha feto protein and Ultrasound . But the confirmation test is done by chromosomal analysis (Karyotype).
Amniotic Fluid Index is used to detect poly/ oligohydramnios ...
Thanks sir
D serum alpha fetoprotein sir
In antenatal period basic screening is msafp then there is increase only they go for fetal karotype sample from chronic villus
11 ans. Mania both nonepinephrin and Serotonin increase
Thnk u so much sir.
Crct answer of challenging qn is option d)serum alpha fetoprotein
Thanks sir 👌 ans is c,it's confirmatory test to detact down syndrome
Sir...answer will be fetal karyotype..because it determines chromosomal abnormality
ANS -21 - C
There are two tests for prenatal screening and determinate test.
By usg we check some sign of foetus like down syndrome but its not confirm by this
AFI is also check by the usg
Serum alpha fetoprotein is produced by foetus but its also a screening test
But we know that down syndrome is trisomy of 21th chromosome so karyotype is diagnostic of determination in this we confirm by check the chromosome of foetus.
Answer21-a fluid back of the neck of fetuscan be detected this test is called NT scanning
Option 4 MSAFP test...if the AFP decreased means it can leads to down syndrome
D. Serum alpha protein test.
Thank you sir
Jiti rho beta
Thank you sir...it is useful
Ans is D. Alpha feto protein... Triplet test is done around 15-18 weeks to rule out out down's syndrome it includes alpha feto protein, beta hcg and estriol
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21)
Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients.
H
Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
D. In serum alpha feto protein test the serum alpha feto protein is decreased in the down syndrome
Option C is right✔
But sir kya fetal kareyotype is a test. I think this a finding of a test.
I think Chorionic vilus sampling is the test for detect the fetal kareyotype
Sir AIIMS NEW DELHI NURSING OFFICER EXAM results ammended hoga kya plz inform me
[24/07, 9:09 PM] shahinaj s: It nuchal translucency
[24/07, 9:10 PM] shahinaj s: At first trimester
Thanks sir
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21)
Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients.
H
Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
SERUM ALPHA FETO PROTEIN
fetal karyotype . it will give a detailed information about chromosomal abnormality
Que. No 21. = ans D serum alfa fetoprotein
Also make video on last year question paper of nimhans
Not available. I tried maximum to get it.
@@sat2careu2.0onlinenursingc2 I have but how I can send it to you
Please send me if you have
Fetal karyotyping
In this the cells of the fetus collected from in utero and analyse by genetic testing for any extra chromosome in 21
This is usually demonstrates the child with down syndrome
C. Fetal karyotope.
Thank you sir
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21)
Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients.
H
Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
Q.21 ans. d
Option C is right✔
ans: d serum alpha fetoprotein
Q.21 C fetal karyotyping will reveal an unexpected finding of a structural chromosome abnormality.
You are right.
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21)
Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients.
H
Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
@@sat2careu2.0onlinenursingc2 thNks for the detail
21_D answer
this is chromosomal disorder
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21)
Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients.
H
Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
C. fetal karyotype
We can diagnose trisomy of 21 chromosome by doing chromosome study
Sir Ji previous ppr update kro na nimhans ka
Maximum extent i tried it. But not available.
Sat 2 Care U 2.0 Online Nursing Channel ok thnks sir
Actually what's the exact syllabus
I send u today. in new video.
D
Option C is right✔
D decrease level afp indicates down syndrome
Option c is right✔
21 St Q
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21)
Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients.
H
Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
C.
21_d
Low alpha fetoprotein leads to down syndrome and high alpha fetoprotein leads to nerual defects
Sir is it correct
Option C is right✔
Thanks sir
@@nursing7863 Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21)
Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients.
H
Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
21ans d
Option C is right✔
A
Fetal karyotype
Usg
D
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21)
Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients.
H
Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
D
Down syndrome is characterized by an extra copy of chromosome 21 (trisomy 21)
Ultrasound can measure nuchal translucency, which increases in Down syndrome. The accuracy tends to vary between examiners and patients.
H
Low levels of AFP may indicate the presence neural tube defects, trisomy 18, or trisomy 21 (Down syndrome). It’s usually combined with other serum marker screenings, and does not definitive diagnosis.
Hi moni
D