Built for the moment
the scan shows something
you didn't expect

The fetal medicine specialist is ScanOFe's core user. Complex, multi-anomaly cases are the daily reality. And these are exactly the cases where cognitive overload is highest and where the consequences of a missed syndrome are most significant.

ScanOFe supports the specialist's existing clinical process at the specific point where it is most strained: converting multiple abnormal findings into a coherent differential that can be communicated to genetics, neonatology, and the patient's family. It does not challenge findings, generate diagnoses, or recommend procedures. It structures the reasoning that the specialist would already apply. Just faster and more completely.

For multidisciplinary fetal board discussions, ScanOFe's structured output serves as a common reference. Phenotype maps, gene linkage, investigation rationale. That all team members can review before the meeting.

Radiologists performing prenatal ultrasound are highly skilled imagers who may not have specialised training in fetal medicine genetics and syndromology. The anomaly scan requires expert image acquisition. But the report must also address what the findings might mean genetically, and what investigations are warranted.

ScanOFe fills the syndromic reasoning gap without requiring the radiologist to become a fetal medicine geneticist. Enter the structural findings you have identified. ScanOFe provides the clinical context that belongs in the report. Potential syndromes to consider, investigations to suggest, and when the case should be escalated to a fetal medicine specialist.

Genetic counselors working in fetal medicine settings need rapid access to prenatal phenotype information. What does this syndrome look like on ultrasound, what is the range of expression, what does the testing pathway look like for this family. This information is scattered across textbooks, OMIM, and institutional knowledge.

ScanOFe's Reverse Mode gives genetic counselors a structured prenatal phenotype map for any syndrome they are counseling around. Organised by organ system, with gestational timing notes. Useful both for pre-test counseling ("here is what the scan should show if this diagnosis is confirmed") and post-result counseling ("here is what to expect on the next scan").

For trainees in fetal medicine and obstetric ultrasound, ScanOFe functions as a structured learning environment. Not a shortcut, but a framework for understanding how experienced clinicians reason through complex cases.

When a trainee encounters an abnormal finding, ScanOFe's structured differential shows the reasoning pathway: which syndromes are associated with this finding, why some rank higher than others, which additional findings would confirm or exclude each candidate. This is explicit reasoning that would otherwise only come from years of supervised practice.

In academic teaching centres, ScanOFe is also used as a case discussion tool. Reverse Mode for pre-session preparation, Forward Mode for live case presentation analysis.