CHROMOAOMAL MICROARRAY 315 (CMA 315K) WITH POC KARYOTYPE in Petlad

Sterling Accuris Diagnostics offers the Chromosomal Microarray 315 (CMA 315k) with POC Karyotype Test in Petlad for genetic testing of people who have multiple congenital anomalies , autism spectrum disorders, or developmental issues. 

Overview of Chromosomal Microarray 315 (CMA 315k) with POC Karyotype Test

Human chromosomes, which are small genetic building blocks with unique genetic combinations, contain all of the genetic material. Birth abnormalities, developmental delays, autism, and other health problems can be caused by even the smallest alteration in the genetic structure of these chromosomes-whether it is an addition, deletion, or exchange. The Chromosomal MicroArray is a high-resolution molecular genetic test that looks for a wide range of chromosomal DNA alterations that could otherwise go unnoticed. CMA scans for extra (duplicated) or missing (deleted) chromosomal regions named copy number changes (CNCs) or copy number variants (CNVs), comprising:

• When the number of chromosomes is less or more than 23.
• Translocations.
• Exorbitant homozygosity,
• Triploidy and additional duplications
• Mosaicism.

For accurate and precise test results head on to Sterling Accuris Diagnostics for the Chromosomal Microarray 315 (CMA 315k) with POC Karyotype Test in Petlad.

Why and when is the Chromosomal Microarray 315 (CMA 315k) with POC Karyotype Test done?

The test is suggested by the doctor since it offers results in as little as 10 days and offers a definite diagnosis for a number of chromosomal defects.

The test is generally advised by the doctor in three phases:

• Prenatal: This would occur between weeks 8 and 13 of pregnancy so that any decisions regarding the treatment of the pregnancy (continuation or termination) may be made with knowledge.
• Postnatal: After delivery, look for any developmental delays, autism spectrum disorders (ASD), seizures, birth defects, numerous congenital anomalies, neuromuscular disease, dysmorphic traits, etc. to make a genetic diagnosis for the child's proper medical care.
• POC (product of conception): The POC could be examined for the purpose of genetic diagnosis to determine the likelihood of recurrence in cases of miscarriage, stillbirth, or medical termination.

Chromosomal Microarray 315 (CMA 315k) with POC Karyotype Test: Main Highlights

• Instructions: No specific preparation is needed.
• Recommended Age: Any age group.
• Sample type for test: Blood sample.

Understanding how to interpret Chromosomal Microarray 315 (CMA 315k) with POC Karyotype Test Reports 

• Normal: No chromosomes are duplicated or missing substantial portions, and there are no extra or extra-large chromosomes.
• Likely pathogenic: A chromosome has an additional or missing portion, which could affect one's health or ability to learn.
• A variant of unknown significance (VUS): Finding a VUS is typical. It is unknown whether the additional or missing chromosome will affect a person's health or ability to learn.
• Regions of Homozygosity (ROH): One or multiple chromosome regions are genetically identical.