Developer Test

17740|Chromosome Analysis, Routine (Amniotic Fluid)

16146|Trisomy FISH screen (13,18,21,X,Y), Amniotic Fluid

16025|Hunter Syndrome (MPS II) : iduronate-2-sulfatase enzyme analysis

Meet Reggie Roper

Reggie has been part of the GGC family for over 18 years. He has short stature, webbing of his hands, pulmonary stenosis, seizures and hydrocephalus along with developmental delay. He carried an initial diagnosis of cardiofaciocutaneous (CFC) syndrome; however, as genetic testing advanced, GGC made the diagnosis of Noon...

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