What is Molecular Karyotyping?
Molecular karyotyping, also known as chromosomal microarray analysis (CMA), is a genetic test used to identify changes in chromosomes, including gains (duplications) or losses (deletions) of chromosome segments. Unlike traditional karyotyping, which visually examines the number and structure of chromosomes under a microscope, molecular karyotyping uses advanced DNA technology to detect smaller chromosomal abnormalities that are not visible by standard methods.

This test is commonly used for diagnosing genetic conditions, particularly those related to developmental delays, autism, and congenital anomalies.

Purpose of Molecular Karyotyping:

1. Detecting Genetic Abnormalities:
   Identifies chromosomal abnormalities such as microdeletions, microduplications, and unbalanced chromosomal rearrangements that may be associated with developmental disorders.

2. Prenatal Diagnosis:
   Used in prenatal settings to assess the genetic health of a fetus, especially when abnormalities are detected through ultrasound or when there's a known risk of chromosomal disorders.

3. Evaluating Developmental Disorders:
   Helps to determine the cause of developmental delays, intellectual disabilities, autism spectrum disorders, and congenital anomalies in children and adults.

When is Molecular Karyotyping Recommended?

• Developmental and Growth Issues:
  When a child has unexplained developmental delays, intellectual disabilities, or congenital physical abnormalities.

• Autism Spectrum Disorders:
  To identify any genetic links to autism or related behavioral and cognitive disorders.

• Prenatal Screening:
  For pregnant women with high-risk factors, including abnormal ultrasound findings or family history of genetic disorders.

Sample Type:

• Blood sample (venipuncture)
• Amniotic fluid (in the case of prenatal diagnosis)
• Buccal swab (sometimes used as an alternative)

Preparation for the Test:

• Fasting: Not required.
• Medications: No special preparation is needed, but inform your doctor of any medications or genetic conditions in the family history.

How the Test Works:

1. A sample of blood or tissue is collected and processed in the lab.
2. The DNA from the sample is analyzed using advanced microarray technology, which scans the entire genome for small deletions, duplications, and other chromosomal abnormalities.
3. Results are analyzed by a genetic specialist, who can determine if there are any chromosomal abnormalities linked to specific health conditions.

SpeedDiagno Booking and Collection:

• Easy Booking: Schedule your Molecular Karyotyping test quickly and easily through the SpeedDiagno app or website.
• Convenient Sample Collection: A professional phlebotomist will collect your blood sample from your home within minutes of booking.
• NABL Certified Labs: Your sample will be analyzed in NABL-certified laboratories, ensuring accuracy and reliability.

Turnaround Time:

• Sample Collection: The blood draw or tissue sample collection takes just a few minutes.
• Results: Typically available within 2-3 weeks, with results accessible through the SpeedDiagno app or website.

Why Choose SpeedDiagno?

• Convenient Booking: Book your test online or through the app.
• At-Home Sample Collection: Enjoy the comfort of having a sample collected at home.
• Certified Labs: Tests are processed at NABL-certified labs, ensuring high accuracy.
• Secure Online Results: Access your results quickly and securely through SpeedDiagno’s online platform.

Support

For any questions or assistance with the Molecular Karyotyping test, SpeedDiagno offers several support options:

• WhatsApp Support:
  Contact us directly through WhatsApp via the SpeedDiagno app or website for quick support.

• Phone Support:
  Call us at 8522 853332 for help from our customer service team.

• In-App Support:
  Use the in-app support feature on the SpeedDiagno app for immediate assistance.

SpeedDiagno provides efficient and reliable testing services with comprehensive support, ensuring a smooth and satisfactory experience