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Wholesome Chromosomal Microarray (CIRCA) Healthcare Provider Statement* April 8, 2016 * Note: This Statement is required, and applies to all cases of Wholesome Chromosomal Microarray testing. Patients
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How to fill out whole-genome chromosomal microarray cma-isca:

01
Begin by gathering all the necessary materials and documents for the completion of the whole-genome chromosomal microarray cma-isca form. This may include the patient's medical history, genetic information, and any relevant test results.
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Fill out the patient's personal information accurately, including their full name, date of birth, gender, and contact information. Make sure to double-check the accuracy of this information as it is crucial for proper identification and communication.
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Provide detailed information about the referring physician, including their name, contact information, and any additional relevant information such as their specialty or affiliation.
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Indicate the reason for performing the whole-genome chromosomal microarray cma-isca test. This can include suspected genetic disorders or abnormalities, developmental delays, intellectual disabilities, or any other indications that warrant further genetic analysis.
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Document the patient's clinical features or symptoms that have led to the decision of conducting the whole-genome chromosomal microarray cma-isca. Describe any relevant medical history, family history, or previous genetic testing results that may be important for a comprehensive evaluation.
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Who needs whole-genome chromosomal microarray cma-isca:

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Individuals with suspected genetic disorders: Whole-genome chromosomal microarray cma-isca is a powerful tool for identifying genetic variations and abnormalities. It can be particularly beneficial for individuals who exhibit symptoms or clinical features that suggest an underlying genetic condition.
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Patients with developmental delays or intellectual disabilities: The whole-genome chromosomal microarray cma-isca can help identify structural changes in the chromosomes that could potentially explain these conditions. Early diagnosis and intervention can significantly improve the management and prognosis of these individuals.
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Individuals with a family history of genetic abnormalities: Whole-genome chromosomal microarray cma-isca can be recommended for individuals with a known family history of genetic disorders. It can aid in the identification of any inherited genetic variations or abnormalities that could contribute to the condition.
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Pre-conception or prenatal screening: Whole-genome chromosomal microarray cma-isca can be recommended as part of pre-conception or prenatal screening to assess the risk of having a child with certain genetic conditions. This screening can help individuals make informed decisions about family planning and prenatal care.
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Whole-genome chromosomal microarray cma-isca is a genetic test that examines the entire genome for chromosomal abnormalities.
Healthcare providers and genetic counselors are required to file whole-genome chromosomal microarray cma-isca for their patients.
Whole-genome chromosomal microarray cma-isca is typically filled out by healthcare providers based on the genetic test results of their patients.
The purpose of whole-genome chromosomal microarray cma-isca is to identify chromosomal abnormalities, such as deletions, duplications, and rearrangements, that may be associated with genetic disorders.
The report must include details of any chromosomal abnormalities identified, as well as recommendations for further testing or management.
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