The CLIA-certified Nemours Molecular Diagnostics Lab serves as a pediatric diagnostic center, providing reliable molecular clinical lab services to diagnose more than 30 genetic diseases.

Located at Nemours/Alfred I. duPont Hospital for Children in Wilmington, Del., our lab specializes in molecular diagnosis of neuromuscular diseases including muscular dystrophy, spinal muscular atrophy, Emery Dreifuss muscular dystrophy and Pelizaeus-Merzbacher disease.

Testing is also available for Barth syndrome, Rett syndrome, Pelizaeus-Merzbacher-like disease, Costello syndrome, CFC syndrome, Feingold syndrome and benign hereditary chorea and many others.