Array Chrome - Chromosomal Microarray Test in Madhapar
50+ booked in last 3 daysTest Overview
Chromosomal Array, Comparative genomic hybridization (CGH) Chromosome array test is a test to identify genetic causes of developmental delay in children. In addition a genetic counselling is provided to parents of the affected child
Overview
The chromosomal array is a laboratory test that can be used to detect genetic abnormalities in an individual. It is a powerful tool that can help diagnose and monitor genetic conditions, both inherited and acquired. Comparative genomic hybridization (CGH) is a test to identify genetic causes of developmental delay in children. In addition, genetic counseling is provided to the parents of the affected child.
What is a chromosomal array?
Chromosomal array analysis involves the use of specialized technology to look at an individual’s entire genome sequence. The analysis provides comprehensive information on abnormal chromosomal changes, including deletions, duplications, and rearrangements of pieces of chromosomes. These data can provide important insights into the underlying cause of a person’s health condition or disorder.
The advantages of chromosomal array testing over traditional testing methods are numerous. For one, it has a higher resolution than traditional methods such as karyotyping or fluorescent in situ hybridization (FISH). In addition, chromosomal array testing is more cost-effective because of its ability to detect multiple types of genetic abnormalities simultaneously. Finally, results from chromosomal array testing can be obtained more quickly than traditional methods because it requires fewer steps in the laboratory process.
Who should get the chromosomal array test done?
- Individuals who have a family history of chromosomal disorders or genetic syndromes.
- Individuals with unexplained multiple miscarriages, stillbirths, or other pregnancy loss.
- Infants or children with developmental delays, growth delays, or physical abnormalities.
- Infants or children with a history of a birth defect or congenital abnormality.
- Individuals with a history of learning difficulties.
- Couples undergoing in vitro fertilization (IVF).
Written by: Dr Vishal Wadhwa, M.D, D.N.B Microbiology, Medical Affairs
Array Chrome - Chromosomal Microarray Test Price in Rajkot
Metropolis Healthcare is a leading diagnostics centre and pathology lab in India equipped with the latest state-of-the-art technologies that provides the Array Chrome - Chromosomal Microarray Test with a clear pricing structure
The price of Array Chrome - Chromosomal Microarray Test in Rajkot is ₹ 17,120
We are committed to deliver accurate and quality results from the best labs in India with complete transparency regarding test cost and turnaround time. No matter where you are, we strive to offer patients high-quality service that is affordable and accessible.
Frequently Asked Questions
To evaluate genetic causes for developmental delay.
This test is for paediatric patients.
Chromosomal array CGH is a sensitive and advanced test with added feature of genetic counseling for detection of subtle and cryptic microdeletions and duplications, specially in Pediatric patients. Detailed clinical history of the patient is required.
How it Works?
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Our Phlebotomists maintain a high standard of safety precautions
Our dedicated team of phlebotomists prioritises your safety before anything else. They implement stringent safety measures to guarantee your well-being during their visit.
Strictly adhering to aseptic techniques, our phlebotomists maintain a sterile environment with thorough sanitization and the use of gloves, masks and face shields. Needles are disposed of with utmost care, following rigorous guidelines to minimise any potential risks. We leave no room for compromise when it comes to personal protective equipment (PPE), ensuring both you and our staff are well protected.
Our phlebotomists collect samples safely
The phlebotomists at Metropolis Healthcare are proficient in safe sample collection. They skillfully and gently draw blood, minimizing any discomfort you may feel. We prioritize your safety by using sterile, single-use needles and barcoded vials to completely eliminate any risk of cross-contamination. Our collection area is carefully sanitized before, during, and after your sample collection.
Samples are processed at high-tech facilities
Metropolis Healthcare takes pride in its state-of-the-art facilities, where your samples are thoroughly processed. Our labs are equipped with cutting-edge machinery with advanced technology, eliminating chances of human error. From the moment your sample arrives at our facility, it undergoes an automated process.
Your samples are stored in clean and secure facilities
We leave no room for compromise when it comes to the storage of your samples. Our storage facilities are regularly cleaned and disinfected, upholding the highest standards of healthcare safety.
Temperature-controlled environments and cooling facilities ensure that your samples remain fresh and the results produced are accurate. Our cutting-edge security measures prevent unauthorized access, guaranteeing the confidentiality of your health data.
Metropolis provides accurate digital reports
Our advanced sample processing machines not only deliver swift results to you but also generate precise digital reports. We provide conclusive diagnoses through meticulous re-checks and repeat specimen analyses, if required, at no extra cost, adding an extra layer of accuracy and dependability. This unique approach sets us apart, earning the trust of top doctors and hospitals across the country.
Your health is our priority, and we spare no effort in our commitment to providing you with the most accurate insights you can rely on.
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Metropolis has a team of 200 senior pathologists and over 2000 technicians delivering diagnostic solutions in the areas of routine, semi specialty and super specialty domains like Oncology, Neurology, Gynaecology, Nephrology and many more.
We offer a comprehensive range of 4000+ clinical laboratory tests and profiles, which are used for prediction, early detection, diagnostic screening, confirmation and/or monitoring of the disease.