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. 2022 Jul 22;13:867337. doi: 10.3389/fgene.2022.867337

TABLE 1.

NBS conditions screened in at least one state but not on RUSP.

Carbamoyl phosphate synthase (CPS) deficiency Fabry disease Hyperornithinemia with gyrate deficiency Nonketotic hyperglycinemia
Congenital cytomegalovirus infection Formiminoglutamic acidemia Hyperornithinemia-hyperammonemiahomocitrullinemia syndrome Ornithine transcarbamylase (OTC) deficiency
Congenital human immunodeficiency virus infection GAMT deficiency Krabbe Disease Prolinemia Type I/Type II
Congenital toxoplasmosis infection Gaucher disease Mucopolysaccharidosis Type II Pyroglutamic acidemia
Ethylmalonic encephalopathy Glucose-6-phosphate dehydrogenase deficiency Niemann Pick disease Zellweger syndrome