{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["15(3)"],"submitter":["Oktem RM"],"pubmed_abstract":["<h4>Background</h4>Hyperphenylalaninemia (HPA) is defined as blood phenylalanine (Phe) levels exceeding the normal values (>120 μmol/L or >2 mg/dL) and is caused by a deficiency in the enzyme phenylalanine hydroxylase (PAH). The widespread screening of Phe levels in newborn screening programs has led to a very high number of patients with HPA.<h4>Methods</h4>The samples were collected at various ages, not at the point of diagnosis. Nine pterin derivatives, including isoxanthopterin, sepiapterin, xanthopterin, primapterin, biopterin, neopterin, 7,8-dihydrobiopterin, 7,8-dihydroneopterin, and tetrahydrobiopterin (BH4), were analyzed in different HPA classes in serum, dried blood spots (DBS), and urine samples. A total of 18 patients, including six classical phenylketonuria (PKU), eight BH4-r"],"journal":["Molecular syndromology"],"pagination":["185-193"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11149980"],"repository":["biostudies-literature"],"pubmed_title":["Pterin Profiling in Serum, Dried Blood Spot, and Urine Samples Using LC-MS/MS in Patients with Inherited Hyperphenylalaninemia."],"pmcid":["PMC11149980"],"pubmed_authors":["Oktem RM","Inci A","Bayrak H","Mavis ME","Yılmaz H","Ezgu FS","Gursu GG","Tumer L","Demir F","Okur I","Biberoglu G"],"additional_accession":[]},"is_claimable":false,"name":"Pterin Profiling in Serum, Dried Blood Spot, and Urine Samples Using LC-MS/MS in Patients with Inherited Hyperphenylalaninemia.","description":"<h4>Background</h4>Hyperphenylalaninemia (HPA) is defined as blood phenylalanine (Phe) levels exceeding the normal values (>120 μmol/L or >2 mg/dL) and is caused by a deficiency in the enzyme phenylalanine hydroxylase (PAH). The widespread screening of Phe levels in newborn screening programs has led to a very high number of patients with HPA.<h4>Methods</h4>The samples were collected at various ages, not at the point of diagnosis. Nine pterin derivatives, including isoxanthopterin, sepiapterin, xanthopterin, primapterin, biopterin, neopterin, 7,8-dihydrobiopterin, 7,8-dihydroneopterin, and tetrahydrobiopterin (BH4), were analyzed in different HPA classes in serum, dried blood spots (DBS), and urine samples. A total of 18 patients, including six classical phenylketonuria (PKU), eight BH4-r","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Jun","modification":"2025-04-18T16:01:25.133Z","creation":"2025-04-07T02:58:30.071Z"},"accession":"S-EPMC11149980","cross_references":{"pubmed":["38841329"],"doi":["10.1159/000535853"]}}