Genetics, birth defects and metabolism

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Treats Gaucher disease, Fabry disease, mucopolysaccharidoses, PKU, galactosemia, glycogen storage disease, inborn errors of metabolism, Marfan syndrome, neurofibromatosis, neurogenetic disorders, phenylketonuria and skeletal dysplasia. Services include diagnosis and counseling.

Head

Joel Charrow, MD

In-house staff

Brad Angle, MD

Barbara K. Burton, MD