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FISH FOR PRE or POSTNATAL DIAGNOSIS CHROMOSOME 13 22 Cost 7000 Rs
FISH FOR PRE or POSTNATAL DIAGNOSIS CHROMOSOME 13 22 Details
FISH for Pre or Postnatal Diagnosis Chromosome 13 22 Cost INR 7000: Symptoms and Diagnosis
Pre or postnatal diagnosis of chromosomal abnormalities is crucial in determining the health of the fetus or newborn. One such diagnostic tool is Fluorescence in situ Hybridization (FISH), which is used to detect specific chromosomal abnormalities. DNA Labs India offers FISH for pre or postnatal diagnosis of chromosome 13 22 at a cost of INR 7000.
What is FISH?
FISH is a molecular diagnostic technique that uses fluorescent probes to bind to specific DNA sequences on chromosomes. The probes are labeled with fluorescent dyes that emit light when exposed to a specific wavelength of light. By using different probes with different colors, FISH can detect multiple chromosomal abnormalities simultaneously.
Why is FISH important for pre or postnatal diagnosis?
FISH is particularly useful for diagnosing chromosomal abnormalities that are not visible under a microscope. It can detect abnormalities that are too small to be seen with traditional cytogenetic techniques and can detect abnormalities in cells that are not dividing. This makes it an important tool for pre or postnatal diagnosis, where a quick and accurate diagnosis is crucial for the health of the fetus or newborn.
Chromosome 13 22 abnormalities
Chromosome 13 and 22 abnormalities are relatively rare, but they can have serious consequences. Abnormalities in chromosome 13 can cause a range of developmental delays and physical abnormalities, while abnormalities in chromosome 22 can cause a range of health problems, including heart defects and developmental delays.
Symptoms of chromosome 13 22 abnormalities
Symptoms of chromosome 13 22 abnormalities can vary depending on the specific abnormality. Some common symptoms include:
- Developmental delays
- Physical abnormalities, such as cleft palate or heart defects
- Intellectual disability
- Seizures
- Behavioral problems
- Growth problems
Diagnosing chromosome 13 22 abnormalities with FISH
FISH is a quick and accurate way to diagnose chromosome 13 22 abnormalities. It can detect abnormalities in cells taken from amniotic fluid or from a blood sample from the newborn. The test is non-invasive and carries minimal risk to the fetus or newborn.
Cost of FISH for pre or postnatal diagnosis of chromosome 13 22
DNA Labs India offers FISH for pre or postnatal diagnosis of chromosome 13 22 at a cost of INR 7000. This includes the cost of the test and the interpretation of the results by a qualified genetic counselor.
Conclusion
FISH is a valuable tool for pre or postnatal diagnosis of chromosomal abnormalities, including chromosome 13 22 abnormalities. It is quick, accurate, and non-invasive, making it an ideal diagnostic tool for determining the health of the fetus or newborn. If you suspect that your child may have a chromosomal abnormality, talk to your doctor about FISH testing.