Logo Need help?
Guest >> Login
Data Management

Case report
Main data  Main data
Molecular genetics  Molecular genetics
Lab findings  Lab findings
Symptoms  Symptoms
Diet/drugs  Diet/drugs
Therapy/development  Therapy/development
References  References

Related data
disease Information  Disease information
Genetic Information  Gene information
Information about metabolic pathways  Pathway information
Substance information  Substance information

Go back to ...
Patient case report | Main data
Patient ID 446
Diagnosis PHENYLKETONURIA (MIM 261600)
Gender m
Age of symptoms onset 0 Day(s)
Age of diagnosis 5.00 Day(s)
Found in newborn screening y
Diagnosis confirmed y
Country Germany
Ethnic origin Mother: German, Father: German
History The patient was found in the newborn screening, in the original hospital tetrahydrobiopterine loading was not performed. Later on the parents moved to Reutlingen, where mutational analysis revealed a biopterine responsive mutation in one allel. BH4 treatment resulted in a decrease of blood phe values from 6 to 2 mg/dl.
Author Friedrich Trefz
Hospital Childrens Hospital Reutlingen
Coauthor(s)
Date of entry 2001-11-19 12:54:02
(c) 2000-2024 RAMEDIS
General: Disclaimer | Webmaster: webmaster@ramedis.de | go top