CYTOGENETIC REQUISITION Patient Information OTHER THAN 2025

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  1. Begin by clearly printing your name in the designated 'Name' section, including both surname and first name.
  2. Fill in your address accurately to ensure proper communication. This is crucial for any follow-up regarding your requisition.
  3. Enter your date of birth in the format DD/MM/YY, and select your sex by marking either 'M' or 'F'.
  4. Provide your health card number as this information is mandatory for processing the specimen.
  5. Complete the 'Ordering Physician' section with the physician's surname and first name who is requesting the test.
  6. Indicate whether the sample is routine or urgent, and if applicable, provide details about any pregnancy at risk.
  7. Specify the testing requested by checking appropriate boxes and providing clinical indications where necessary.

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Cytogenetics is a branch of biology focused on the study of chromosomes and their inheritance, especially as applied to medical genetics. Chromosomes are microscopic structures containing DNA that reside within the nucleus of a cell.
Cytogenetic testing is the examination of chromosomes to determine chromosome abnormalities such as aneuploidy and structural abnormalities. A normal human cell contains 23 pairs of chromosomes, including 22 pairs of autosomes and a pair of sex chromosomes (XX or XY).
There are three major methods of cytogenetic testing: Routine karyotyping. Fluorescent in situ hybridisation (FISH) Comparative genomic hybridisation (CGH) and array comparative genomic hybridisation (aCGH).
In summary, cytogenetic tests analyze the structure and number of chromosomes, while molecular genetic tests focus on studying specific genes and DNA sequences.
Cytogenetic testing is recommended for individuals with certain conditions, such as congenital disabilities, developmental delays, intellectual disability, autism, or certain types of cancer.