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Chromosomes 13 and 21 Test Cost

Original price was: 1,600 د.إ.Current price is: 1,200 د.إ.

-25%

The “Chromosomes 13 and 21 Test” is a specialized genetic screening conducted at DNA Labs UAE, designed to identify any abnormalities in chromosomes 13 and 21. These chromosomes are significant as their anomalies are linked to certain genetic disorders. For example, trisomy 13, also known as Patau syndrome, is associated with chromosome 13, while trisomy 21 leads to Down syndrome, related to chromosome 21. The test is crucial for early detection, allowing for better preparation and management of potential health issues associated with these chromosomal abnormalities.

DNA Labs UAE offers this testing service for a cost of 1200 AED. The lab utilizes advanced genetic testing technologies to ensure accurate and reliable results. This test is particularly recommended for expectant parents or individuals with a family history of genetic disorders. By opting for this test, one can gain valuable insights into their genetic health or that of their unborn child, facilitating informed medical and personal decisions.

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  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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CHROMOSOMES 13 and 21 Test

Test Name: CHROMOSOMES 13 and 21 Test

Components: Sterile container / Sterile Normal Saline Container / Sodium heparin Vacutainer (2ml)

Price: 1200.0 AED

Sample Condition: Amniotic fluid / Chorionic villi / Cord blood

Report Delivery: 3-4 days

Method: FISH

Test Type: Genetics

Doctor: Oncology

Test Department:

Pre Test Information: CHROMOSOMES 13 & 21 can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Test Details

Chromosomes 13 and 21 are two of the 23 pairs of chromosomes found in humans. They are both autosomes, meaning they are not involved in determining the sex of an individual.

Chromosome 13:

  • It is one of the largest chromosomes in the human genome, consisting of about 114 million base pairs.
  • Mutations or abnormalities in chromosome 13 can lead to various genetic disorders, such as trisomy 13 (also known as Patau syndrome), which is characterized by severe developmental issues and multiple physical abnormalities.

Chromosome 21:

  • It is the smallest human chromosome, consisting of about 48 million base pairs.
  • The most well-known abnormality associated with chromosome 21 is trisomy 21, also known as Down syndrome. Individuals with Down syndrome have an extra copy of chromosome 21, resulting in developmental delays, intellectual disability, and distinct physical features.

Both chromosomes 13 and 21 play important roles in the overall functioning and development of an individual, and abnormalities in these chromosomes can have significant impacts on health and well-being.

Test Name CHROMOSOMES 13 and 21 Test
Components Sterile container / Sterile Normal Saline Container / Sodium heparin Vacutainer (2ml)
Price 1200.0 AED
Sample Condition Amniotic fluid \/ Chorionic villi \/ Cord blood
Report Delivery 3-4 days
Method FISH
Test type Genetics
Doctor Oncology
Test Department:
Pre Test Information CHROMOSOMES 13 & 21 can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

Chromosomes 13 and 21 are two of the 23 pairs of chromosomes found in humans. They are both autosomes, meaning they are not involved in determining the sex of an individual.

Chromosome 13:

– It is one of the largest chromosomes in the human genome, consisting of about 114 million base pairs.

– Mutations or abnormalities in chromosome 13 can lead to various genetic disorders, such as trisomy 13 (also known as Patau syndrome), which is characterized by severe developmental issues and multiple physical abnormalities.

Chromosome 21:

– It is the smallest human chromosome, consisting of about 48 million base pairs.

– The most well-known abnormality associated with chromosome 21 is trisomy 21, also known as Down syndrome. Individuals with Down syndrome have an extra copy of chromosome 21, resulting in developmental delays, intellectual disability, and distinct physical features.

Both chromosomes 13 and 21 play important roles in the overall functioning and development of an individual, and abnormalities in these chromosomes can have significant impacts on health and well-being.