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Újszülöttkori szűrés - Első szegedi továbbképző összejövetel (Szeged, 2011.06.27-29.)

TimeProgram
10:00 - 16:00

NEWBORN SCREENING - PHENYLKETONURIA, GALACTOSEMIA, HYPOTHYREOSIS AND CONGENITAL ADRENAL HYPERPLASIA

1ST Workshop within the frame of the HURO project SCREENGEN

27-29 June 2011

Programme:

Monday, 27.06.2011

Place: Library, Dept. Pediatrics, University of Szeged, Koranyi fasor 14-15, Szeged, Hungary

10.00 Opening
Prof. Dr. Sandor Turi
10.15-10.55. Phenylketonuria and other hyperphenylalaninemias
Dr. Gabor Racz
10.55.-11.25. Screening for phenylketonuria - laboratory methods
Dr. Peter Monostori
Discussion
Break
11.45.12.15. Galactosemia
Dr. Gabor Racz
12.15.-12.35. Screening for galactosemia - laboratory methods
Dr. Melinda Rozsa
Discussion
Break
14.00-14.40. Hypothyreosis and congenital adrenal hyperplasia
Dr. Balazs Gellen
14.40-15.10 Screening for hypothyreosis and CAH, second-tier testing – laboratory methods
Dr. Peter Monostori
Discussion
Break
15.30.-16.00. Newborn screening (sample collection, data evaluation, reporting)
Dr. Eszter Karg

Tuesday and Wednesday, 28.-29.06.2011

Place: Screening Laboratory, Dept. Pediatrics, University of Szeged

8.00-14.00. Introduction to the ELISA methods (PKU, galactosemia, hypothyreosis) and the
MS/MS analysis (laboratory practice in the Metabolic Screening Lab, Dept. Pediatrics,
Univ. Szeged, for 2 colleagues)