A Family’s Journey with Rare Disease: Molybdenum Cofactor Deficiency Type A

A Family’s Journey with Rare Disease: Molybdenum Cofactor Deficiency Type A

The Dahab family moved to Ohio to be close to their “second family” at Nationwide Children’s Hospital. Thanks to Nationwide’s excellence in maternal fetal medicine and fetal imaging, a world-class NICU, access to genome sequencing, and rare disease experts, their boys are living longer and better lives.