Get the free Cytogenetics - Warde Medical Laboratory

WARD MEDICAL LABORATORY PRENATAL GENETIC TEST REQUISITION 7342140300 8007609969 Fax: 7342140399 Patient Information *Name: Last First MI Date of Birth: / / Patient ID: Specimen ID: *Referring Physician:

How to fill out cytogenetics - warde medical

How to fill out cytogenetics - Warde Medical:

1. Obtain the necessary forms: Start by acquiring the cytogenetics forms from Warde Medical. These forms are typically provided by the laboratory performing the testing.
2. Provide patient information: Fill in the patient's personal information such as name, age, gender, and contact details. It is important to ensure that this information is accurately recorded to avoid any miscommunication.
3. Medical history and clinical information: In this section, include relevant details about the patient's medical history, symptoms, and any previous genetic testing or procedures. This information helps provide context for the cytogenetic testing and assists the laboratory in interpreting the results effectively.
4. Reason for testing: Indicate the reason for conducting the cytogenetic testing. This could range from evaluating the presence of genetic abnormalities to diagnosing certain genetic disorders or assisting in prognosis and treatment decisions.
5. Specimen collection details: Specify the type of sample that will be collected for the cytogenetic analysis. It could be blood, bone marrow, tissue, or other biological samples. Ensure that the appropriate sample collection procedure is followed to maintain the integrity of the specimen.
6. Ordering physician information: Provide the ordering physician's name, contact information, and any additional relevant details. This helps to establish clear communication between the laboratory and the healthcare provider, ensuring the accurate and timely delivery of test results.

Who needs cytogenetics - Warde Medical:

1. Patients with suspected genetic abnormalities: Cytogenetic testing may be necessary for individuals who are showing signs and symptoms suggestive of genetic disorders. These tests can help diagnose conditions such as Down syndrome, Turner syndrome, or other chromosomal abnormalities.
2. Individuals with a family history of genetic disorders: If there is a known family history of genetic disorders, cytogenetic testing can be useful in assessing the risk of inheriting the condition or identifying any underlying genetic abnormalities that might be impacting the family members.
3. Patients undergoing infertility evaluation: Cytogenetic testing is sometimes recommended for couples undergoing fertility evaluations. It helps identify chromosomal abnormalities that may be affecting their ability to conceive or carry a pregnancy to term.
4. Individuals with cancer: Cytogenetic testing can be utilized in cancer patients to evaluate specific chromosomal abnormalities associated with certain types of cancer. This information can aid in prognosis, treatment decisions, and monitoring disease progression.
5. Prenatal testing: Pregnant women may undergo cytogenetic testing, particularly through techniques like amniocentesis or chorionic villus sampling, to identify any genetic abnormalities or chromosomal disorders in the developing fetus.

It is essential to consult with a healthcare professional to determine if cytogenetic testing is needed in specific cases, as they can provide personalized recommendations based on an individual's medical history and symptoms.

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