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National University Hospital 5 Lower Kent Ridge Road Singapore 119074 www.nuh.com.sg Tel: (65) 6772 4384 / 2512MEMORANDUM To:All Laboratory Serfdom:Cytogenetics laboratory and Molecular Diagnosis

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How to fill out chromosomal microarray post-natal

01

Obtain a sample of blood from the patient

02

Extract DNA from the blood sample

03

Label the DNA with fluorescent dyes

04

Hybridize the DNA to a microarray chip

05

Scan the microarray chip for genetic variations

06

Analyze the data and interpret the results

Who needs chromosomal microarray post-natal?

01

Individuals with unexplained developmental delays or intellectual disabilities

02

Individuals with multiple congenital anomalies

03

Individuals with a family history of genetic disorders

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What is chromosomal microarray post-natal?

Chromosomal microarray post-natal is a genetic test that looks for extra or missing chromosomal segments that could be the cause of a developmental delay, intellectual disability, autism, or other birth defects.

Who is required to file chromosomal microarray post-natal?

Healthcare providers or genetic counselors are usually responsible for ordering and interpreting chromosomal microarray post-natal testing.

How to fill out chromosomal microarray post-natal?

Chromosomal microarray post-natal testing involves taking a blood sample or a tissue sample and sending it to a laboratory for analysis.

What is the purpose of chromosomal microarray post-natal?

The purpose of chromosomal microarray post-natal is to identify genetic abnormalities that may be contributing to a person's developmental delay, intellectual disability, or birth defects.

What information must be reported on chromosomal microarray post-natal?

The report typically includes details on any genetic variants found, their significance, and recommendations for further evaluation or management.

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