[Maternal phenylketonuria. Fölling's disease in pregnancy as the cause of congenital microcephaly and mental retardation].
Explore the source record for details and available documents.
Child, Preschool↗
Biomedical subjects
E Wamberg
Publications and source records attributed to E Wamberg.
Successful outcome of pregnancy in a phenylketonuric woman after low-phenylalanine diet introduced before conception.
Explore the source record for details and available documents.
Female↗
[Genetic disease as the cause of mental retardation. I. Familial mental retardation].
Explore the source record for details and available documents.
Humans↗
Fasting serum phenylalanine in untreated institutionalised patients with phenylketonuria.
Explore the source record for details and available documents.
Adolescent↗
On indications for treatment of the hyperphenylalaninemic neonate.
Of 488 006 neonates tested by Guthrie screening 58 showed values above 2.5 mg/100 ml. Thirty-two showed values between 2.5 mg/100 ml and 15 mg/100 ml. Eighteen of these infants appeared to have phenylketonuria (PKU) and fourteen to have persistent hyperphenylalaninemia (HPA). Neither the initial Guthrie test-value nor the confirmatory test were able to differentiate between these two conditions. Consequently a phenylalanine restricted diet is started in any child with serumphenylalanine values exceeding 10 mh/100 ml (605 micronmol/l). The data show that the course of the dietary tolerance of phenylalanine and a 24-hour phenylalanine load test will differentiate infants with PKU from those with HPA.
Denmark↗
[Oligophrenia as a subject in medical education].
Explore the source record for details and available documents.
Curriculum↗
Incidence and distribution of pku-cases in Denmark.
Explore the source record for details and available documents.
Child, Preschool↗