NARP-Syndrom
Parent facilities 0
Genetic Advices 1
MGZ Medizinisch Genetisches Zentrum München
                    Bayerstr. 3-5
                    80335 München
                
                             089 30908860
                            
 089 309088666
                            
                                
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Care facilities 5
Zentrum für seltene Stoffwechselerkrankungen der Medizinischen Hochschule Hannover
Zentrum für Seltene Erkrankungen Hannover Medizinische Hochschule Hannover
                    Carl-Neuberg-Straße 1
                    30625 Hannover
                
Zentrum für angeborene pädiatrische Stoffwechselerkrankungen am LMU Klinikum München
Care for Rare Center am Dr. von Haunerschen Kinderspital am LMU Klinikum München Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum
                    Lindwurmstr. 4
                    80337 München
                
- Glycogen storage disease
- Very long chain acyl-CoA dehydrogenase deficiency
- Phenylketonuria
- Galactosemia
- Medium chain acyl-CoA dehydrogenase deficiency
- Tyrosinemia type 1
- Mitochondrial disease
- Disorder of carnitine cycle and carnitine transport
- Fabry disease
- Glutaryl-CoA dehydrogenase deficiency
- Maple syrup urine disease
- Disorder of urea cycle metabolism and ammonia detoxification
Zentrum für mitochondriale Erkrankungen am LMU Klinikum München
Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum
                    Ziemssenstraße 1
                    80336 München
                
                             089 440057400
                            
 089 440057402
                            
                                
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- Mitochondrial DNA depletion syndrome
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- MELAS
- Mitochondrial neurogastrointestinal encephalomyopathy
- Leber hereditary optic neuropathy
- Pearson syndrome
- Maternally-inherited diabetes and deafness
- Barth syndrome
- Mitochondrial myopathy
- Mitochondrial membrane protein-associated neurodegeneration
- Kearns-Sayre syndrome
- Coenzyme Q10 deficiency
- Recessive mitochondrial ataxia syndrome
- MERRF
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
- Pantothenate kinase-associated neurodegeneration
- Rare ataxia
- Atypical pantothenate kinase-associated neurodegeneration
- Neuroferritinopathy
- Mitochondrial disease
- Infantile neuroaxonal dystrophy
- Neurodegeneration with brain iron accumulation
- Classic pantothenate kinase-associated neurodegeneration
- Myasthenia gravis
- Leukodystrophy
- Huntington disease
- Hereditary spastic paraplegia
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
Zentrum für metabolische Erkrankungen (ZME)-Tübingen
                    Paul-Ehrlich-Strasse 23
                    72076 Tübingen
                
                             07071 7049000
                            
 07071 7049002
                            
                                
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