MediFind found 7 doctor with experience in Galactose Epimerase Deficiency near Gelderland, NL. Of these, 3 are Experienced, 2 are Advanced and 2 are Distinguished.
Mirian Janssen practices in Nijmegen, Netherlands. Ms. Janssen is rated as a Distinguished expert by MediFind in the treatment of Galactose Epimerase Deficiency. Her top areas of expertise are Classic Galactosemia, Ballinger-Wallace Syndrome, MELAS Syndrome, Galactosemia, and Kidney Transplant.
Maaike De Vries practices in Nijmegen, Netherlands. Ms. De Vries is rated as a Distinguished expert by MediFind in the treatment of Galactose Epimerase Deficiency. Her top areas of expertise are Classic Galactosemia, Galactose Epimerase Deficiency, Galactokinase Deficiency, and Galactosemia.
Saskia Wortmann practices in Nijmegen, Netherlands. Ms. Wortmann is rated as an Advanced expert by MediFind in the treatment of Galactose Epimerase Deficiency. Her top areas of expertise are Classic Galactosemia, Infantile Neutropenia, Von Gierke Disease, Agranulocytosis, and Bone Marrow Transplant.
Dirk Lefeber practices in Nijmegen, Netherlands. Mr. Lefeber is rated as an Advanced expert by MediFind in the treatment of Galactose Epimerase Deficiency. His top areas of expertise are DPAGT1-CDG, ALG1-CDG, PMM2-Congenital Disorder of Glycosylation, PGM1-CDG, and Leg or Foot Amputation.
Marek Noga practices in Nijmegen, Netherlands. Mr. Noga is rated as an Experienced expert by MediFind in the treatment of Galactose Epimerase Deficiency. His top areas of expertise are Classic Galactosemia, Delayed Growth, Galactosemia, and Galactokinase Deficiency.
Fokje Zijlstra practices in Nijmegen, Netherlands. Zijlstra is rated as an Experienced expert by MediFind in the treatment of Galactose Epimerase Deficiency. Their top areas of expertise are Sialuria, Sialic Acid Storage Disease, Galactosemia, and Classic Galactosemia.
Ron Wevers practices in Nijmegen, Netherlands. Mr. Wevers is rated as an Experienced expert by MediFind in the treatment of Galactose Epimerase Deficiency. His top areas of expertise are Xanthoma, Cerebrotendinous Xanthomatosis, Cutis Laxa, and Autosomal Recessive Cutis Laxa Type 1.
Last Updated: 01/09/2026