Women Health Dulwich offers comprehensive panorama test in London by highly experienced experts. 

How is Panorama different?

• Panorama is the only NIPT that can tell the difference between the mother’s and the baby’s DNA, which results in:
• Fewer false positives and fewer false negatives1,2,3
• The highest reported gender accuracy of any NIPT (gender reporting is optional*)1,2,3
• The ability to detect triploidy, a severe chromosomal abnormality that can result in serious pregnancy complications if unmonitored 6,7
• The ability to distinguish whether twins are identical or fraternal – this information can impact the care plan your healthcare provider creates

What does Panorama screen for?

Singleton pregnancies

• Trisomy 21 (Down syndrome)
• Trisomy 18 (Edwards syndrome)
• Trisomy 13 (Patau syndrome)
• Triploidy
• Monosomy X (Turner syndrome)
• Sex chromosome trisomies
• Microdeletions, including 22q11.2 deletion
• syndrome (optional)
• Gender (optional)*

Twin pregnancies

Identical or fraternal twins:

• Trisomy 21 (Down syndrome)
• Trisomy 18 (Edwards syndrome)
• Trisomy 13 (Patau syndrome)
• Gender of each twin (optional)

If our screening finds that your twins are identical, Panorama can additionally screen for:

• Monosomy X (Turner syndrome)
• Sex chromosome trisomies
• 22q11.2 deletion syndrome (optional)

Egg donor or surrogate pregnancies

• Trisomy 21 (Down syndrome)
• Trisomy 18 (Edwards syndrome)
• Trisomy 13 (Patau syndrome)
• Gender (optional)*

What are microdeletions?

A small, missing piece of a chromosome is called a microdeletion. Unlike Down syndrome, which occurs more frequently in mothers who are 35 and older, microdeletions occur in pregnancies at the same rate for mothers of any age. Panorama screens for five microdeletion syndromes associated with serious health problems:

• 22q11.2 deletion (DiGeorge) syndrome
• 1p36 deletion syndrome
• Angelman syndrome
• Prader-Willi syndrome
• Cri-du-chat syndrome

Vistara Single-Gene NIPT

Vistara is the most comprehensive prenatal single-gene screening test for serious genetic conditions. These conditions, which affect quality of life, could benefit from early intervention and might otherwise go undetected.

Vistara tests for 25 serious genetic conditions with a blood draw from the mother. Most results will be returned to a clinician within 3-4 weeks.

Screen for 25 autosomal dominant and X-linked conditions across 30 genes with Vistara single-gene NIPT

Combined incidence greater than Down syndrome

Provide clinically actionable information

Many single-gene conditions benefit from early intervention

Inform decisions for pregnancy and delivery management, early interventions, and patient education to ensure every child reaches their full potential

Perform testing with ease and get clear results

No paternal and/or egg-donor* sample necessary

Find conditions other screening modalities would miss until after the window for critical intervention

Book your webinar to learn more about Vistara Single Gene NIPT