Researchers compared genetic markers across multiple syndromes to identify shared mutations.

Doctors recognized the syndrome early, allowing for targeted treatment and better prognoses.

The research team implemented syndromic surveillance to detect emerging patterns of illness based on reported symptoms.

The patient's syndromal presentation complicated the diagnostic process for the medical team.

The patients' symptoms syndromally suggested a broader neurodevelopmental disorder that required multidisciplinary assessment.

The syndromed patient required extra support during their recovery.

The researchers syndromically analyzed the cluster of symptoms to identify a unifying diagnosis.

In recent years, syndromics has emerged as a crucial field for classifying and understanding complex medical conditions characterized by multiple symptoms.

Researchers compared multiple Gorlin's syndromes to identify common genetic mutations.

Journalists wrote articles about potential China syndromes after the reactor incident, questioning safety protocols.