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Case report
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Molecular genetics  Molecular genetics
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Patient case report | Main data
Patient ID 406
Diagnosis PHENYLKETONURIA (MIM 261600)
Gender m
Age of symptoms onset
Age of diagnosis 6.00 Day(s)
Found in newborn screening y
Diagnosis confirmed y
Country Germany
Ethnic origin Mother: German, Father: German
History Diagnosis of PKU was made already prenataly for second child (brother of ID 405) of healthy German parents. After birth, diagnosis was confirmed by elevated phe-levels. Therapy with phe-restricted diet led to quite normal development.
Author Friedrich Trefz
Hospital Childrens Hospital Reutlingen
Coauthor(s)
Date of entry 2001-10-31 16:58:41
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