High resolution Cytoscan molecular karyotype – Neoscreen testing
High resolution – high sensitivity – HD Karyotype Molecular Cytoscan is the most comprehensive non-invasive prenatal screening. It is performed with Affimetrix’s cutting-edge technology, used at, Mayo Clinic, Baylor Institute, Lab Corp, etc.
Detection of all known syndromes is performed, with analysis of 12,000 gene-transmitted diseases and coverage of the entire genome.
It is the test of choice when there are:
- Abnormal 1st or 2nd trimester
- High-risk pregnancy due to advanced age
- Suspensions
- Elimination products
- Need to investigate childhood neurodevelopmental diseases
It is recommended in all cases of high-risk pregnancies and especially in late-term pregnancies, as a first choice, compared to amniocentesis, even compared to non-invasive prenatal testing (Harmony test, Nifty test).
The molecular karyotyping of Cytoscan HD – Affymetrix is done with the approval of the FDA of America (when combined with the Affymetrix DX scanner)
Attention
It is always important to consult a qualified health professional before having any genetic testing to make sure you fully understand the conditions being tested, as well as the explanation of the results.
Cost 540 euros
Pre-coordination is required for the control
Selected information from sources:
- MayoClinic.org
- Labtestsonline.org
- Interpretation of Diagnostic Tests – J.Wallach
The personalization of the check-up takes into account multiple parameters of personal and family history.
Depending on the case, the selection of tests may require some that are not mentioned on this page.
The exact selection is the responsibility of your attending physician.
Edited by: Ioannis Gratsias, Lab Director / Clinical Biochemist
e – Booking via Doctor Anytime at: Cardiologist – Neurologist– Diagnostic Tests
Informative Blogs: checkup.com.gr – nosileftis24.gr– syntagografisis.gr – testcovid.gr
Biopathology Diagnostic Center – Athens | Medical Center Check Up Medicus | Checkup – Allergy Test – Blood Tests – Prices – Cost – Covid-19 Test | EOPYY.
Panormou Diagnostic Center 40, Ampelokipoi | Diagnostic Center Alexandra Avenue 110 | Diagnostic Center Prykiponnision 24, Gyzi Polygono Kypseli
At Check-Up Medicus you can come for a blood draw without an appointment
Molecular karyotyping, also known as Cytoscan, is an important testing procedure used to detect genetic abnormalities and pathological changes in the human body. This test is particularly important for the diagnosis and monitoring of many genetic diseases, as well as for the prevention and personalised treatment of many cancers.
The process involves the analysis of a person’s genomic material, known as the genetic code or DNA. This analysis can reveal multiple pathological changes, such as changes in the structure of chromosomal material, duplicate copies of DNA fragments, deletions or additional DNA fragments, and mutations that may be associated with various diseases.
It can be used in various fields of medicine, including genetic medicine, oncology, gynaecology and paediatrics. Let’s look at its use in different situations:
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Genetic abnormalities: The Cytoscan molecular karyotype can detect genetic abnormalities such as Dawn syndromes, Edwards syndrome, Turner syndrome, as well as sequences or duplicate copies of genomic segments.
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Cancer: used to detect genetic mutations associated with the pathogenesis of cancer. This can help in the prevention, diagnosis and treatment of cancer, as well as in the development of personalised treatments.
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Reproductive Health: In gynecology, the Cytoscan molecular karyotype can be used to detect genetic abnormalities associated with reproductive problems.
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Diagnosis of childhood diseases: in paediatrics, the Cytoscan molecular karyotype can be used to diagnose genetic diseases and conditions that affect children from an early age.
The Cytoscan molecular karyotype procedure usually involves collecting a DNA sample from the patient, usually through blood or a patch. The DNA is then analysed using modern molecular biology techniques such as microarray polymorphism analysis (SNP), copy number analysis (CNA) and mutation detection.
In summary, the Cytoscan molecular karyotype is a powerful tool for the diagnosis and monitoring of genetic diseases and conditions. Its use is often combined with other diagnostic methods for a more complete picture of the patient’s health and the appropriate treatment of health problems.
