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KARYOTYPE AND MICROARRAY REQUEST FORM Cytogenetics Laboratory UNC Hospitals; McClendon Laboratories and Department of Pediatrics st Room 1071, 1 Floor Memorial Hospital 101 Manning Drive, CB# 7487
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How to fill out karyotype and microarray request
How to fill out a karyotype and microarray request:
01
Start by obtaining the necessary paperwork or forms for the karyotype and microarray request. These forms can usually be obtained from a healthcare provider or laboratory.
02
Begin by providing your personal information on the form. This may include your name, date of birth, contact information, and any relevant medical history.
03
Next, provide information about the patient for whom the karyotype and microarray analysis will be conducted. Include the patient's name, date of birth, and any other pertinent information such as medical conditions or symptoms.
04
Indicate the reason for the karyotype and microarray request. This may include a suspected genetic disorder, developmental delays, or a family history of certain conditions.
05
Provide any additional details or specific instructions for the laboratory. This may include any specific genetic tests that need to be conducted, preferred testing methods, or any additional concerns or questions.
06
Ensure that all necessary signatures and authorizations are included on the form. This may include consent for testing and authorization for release of the results to specific healthcare providers.
07
Double-check all the information provided on the form for accuracy and completeness before submitting it to the laboratory. Any errors or missing information could potentially delay the testing process.
Who needs a karyotype and microarray request?
01
Individuals who are experiencing unexplained developmental delays or intellectual disabilities may benefit from a karyotype and microarray analysis. These tests can help identify any genetic abnormalities or chromosomal disorders that may be contributing to these conditions.
02
Individuals with a suspected genetic disorder, based on their medical history or symptoms, may also require a karyotype and microarray analysis. These tests can provide important information about the presence of certain genetic mutations or abnormalities.
03
Individuals who have a family history of certain genetic conditions or disorders may be advised to undergo a karyotype and microarray analysis. This can help determine if they are at an increased risk of developing the same condition or passing it on to their children.
04
In some cases, prenatal testing may also include a karyotype and microarray analysis. This can help identify any chromosomal abnormalities or genetic disorders in the developing fetus.
Overall, the karyotype and microarray request is necessary for individuals who require genetic testing to determine the presence of any genetic abnormalities or disorders.
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