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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 405
Diagnosis PHENYLKETONURIA (MIM 261600)
Gender f
Age of symptoms onset
Age of diagnosis 7.00 Day(s)
Found in newborn screening y
Diagnosis confirmed y
Country Germany
Ethnic origin Mother: German, Father: German
History The first child of healthy German parents was found in th newborn screening program with increased phe-level. Therapy with phe-restricted diet. Normal development, no clinical symptoms. Sister of ID 406.
Author Friedrich Trefz
Hospital Childrens Hospital Reutlingen
Coauthor(s)
Date of entry 2001-10-31 15:18:33
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