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TRAINEE HANDBOOK 2019Genetic Pathology (Medical Genomics)It is essential to read this Handbook in conjunction with the Trainee Handbook Administrative requirements which is relevant to all trainees.
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How to fill out genetic pathology medical genomics
How to fill out genetic pathology medical genomics
01
Gather the necessary patient information, including medical history, family history, and any existing genetic test results.
02
Consult with a genetic counselor or medical geneticist to discuss the need for genetic pathology medical genomics and determine the most appropriate tests to order.
03
Obtain consent from the patient or legal guardian to perform genetic testing.
04
Collect the required biological samples, such as blood, saliva, or tissue, following standard procedures.
05
Prepare the collected samples for analysis, ensuring proper labeling and documentation.
06
Submit the samples to a reputable genetic pathology laboratory for testing.
07
Await the results from the laboratory, which may take several weeks.
08
Once the results are available, interpret them in conjunction with the patient's clinical information.
09
Discuss the findings with the patient and their healthcare team, providing appropriate genetic counseling and guidance for further management or treatment.
10
Document the test results and relevant information in the patient's medical records for future reference.
Who needs genetic pathology medical genomics?
01
Genetic pathology medical genomics may be needed by individuals with suspected or known genetic disorders.
02
This includes patients with a family history of inherited diseases, recurrent pregnancy loss, multiple congenital anomalies, developmental delays, or unexplained chronic diseases.
03
It may also be beneficial for individuals planning a pregnancy, as it can provide information on potential genetic risks that may affect their offspring.
04
Healthcare professionals, such as geneticists, oncologists, and fertility specialists, may also require genetic pathology medical genomics to assist in diagnosis, treatment decision-making, and genetic counseling.
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