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KJ Muldoon, a 10-month-old baby, was diagnosed with the genetic disease carbamoyl-phosphate synthetase 1 deficiency after he ...
KJ Muldoon, a 10-month-old baby diagnosed with a rare metabolic disease called CPS1 has been at the Children's Hospital of ...
KJ Muldoon, a 10-month-old baby diagnosed with a rare metabolic disease called CPS1 has been at Children Hospital of ...