Dr. Salinas tapped the monitor, zooming in on the complex corporate and genetic markers flashing on the high-definition diagnostic feed.
“This is a monochorionic, multi-amniotic presentation,” Dr. Salinas explained smoothly, her tone laced with absolute clinical certainty. “Laura is carrying identical triplets. And due to a highly rare, dominant chromosomal mutation visible in the embryonic cell division, these children carry a specific, unique genetic marker—a vascular variance that can only be inherited from a direct paternal bloodline with a history of congenital cardiac framing.”
Diego frowned, his arrogant head-of-the-household facade tightening into a knot of sudden anxiety. “What… what does that mean? What kind of marker?”
