Classic glucose transporter type 1 deficiency syndrome
All Entries 4
Sozialpädiatrisches Zentrum am Klinikum Aschaffenburg-Alzenau
Am Hasenkopf 1
63739 Aschaffenburg
06021 323701
06021 323702
Website
Email
Zentrum für angeborene Stoffwechselerkrankungen am Universitätsklinikum Freiburg
Freiburg Zentrum für Seltene Erkrankungen (FZSE) Universitätsklinikum Freiburg
Mathildenstraße 1
79106 Freiburg
- Glucose-galactose malabsorption
- Disorder of branched-chain amino acid metabolism
- Disorder of fatty acid oxidation and ketone body metabolism
- Disorder of fructose metabolism
- Glycogen storage disease
- Disorder of ketolysis
- Maple syrup urine disease
- Disorder of galactose metabolism
- Gluconeogenesis disorder
- Hereditary fructose intolerance
- Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
Website
Email
- Mitochondrial membrane protein-associated neurodegeneration
- Hereditary spastic paraplegia
- Huntington disease
- Infantile neuroaxonal dystrophy
- COASY protein-associated neurodegeneration
- Rare ataxia
- Neurodegeneration with brain iron accumulation
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial disease
- Beta-propeller protein-associated neurodegeneration
- Leukodystrophy
- Atypical pantothenate kinase-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Neuroferritinopathy
Förderverein Glukosetransporter(GLUT1)-Defekt e.V.
Stolzenhagener Straße 17
12679
Berlin
Parent facilities 0
Genetic Advices 0
Care facilities 3
Sozialpädiatrisches Zentrum am Klinikum Aschaffenburg-Alzenau
Am Hasenkopf 1
63739 Aschaffenburg
06021 323701
06021 323702
Website
Email
Zentrum für angeborene Stoffwechselerkrankungen am Universitätsklinikum Freiburg
Freiburg Zentrum für Seltene Erkrankungen (FZSE) Universitätsklinikum Freiburg
Mathildenstraße 1
79106 Freiburg
- Glucose-galactose malabsorption
- Disorder of branched-chain amino acid metabolism
- Disorder of fatty acid oxidation and ketone body metabolism
- Disorder of fructose metabolism
- Glycogen storage disease
- Disorder of ketolysis
- Maple syrup urine disease
- Disorder of galactose metabolism
- Gluconeogenesis disorder
- Hereditary fructose intolerance
- Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
Website
Email
- Mitochondrial membrane protein-associated neurodegeneration
- Hereditary spastic paraplegia
- Huntington disease
- Infantile neuroaxonal dystrophy
- COASY protein-associated neurodegeneration
- Rare ataxia
- Neurodegeneration with brain iron accumulation
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial disease
- Beta-propeller protein-associated neurodegeneration
- Leukodystrophy
- Atypical pantothenate kinase-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Neuroferritinopathy
Supportgroups 1
Förderverein Glukosetransporter(GLUT1)-Defekt e.V.
Stolzenhagener Straße 17
12679
Berlin