NARP syndrome
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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
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
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- Atypical pantothenate kinase-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Mitochondrial disease
- Classic pantothenate kinase-associated neurodegeneration
- Neuroferritinopathy
- Infantile neuroaxonal dystrophy
- Huntington disease
- Rare ataxia
- Pantothenate kinase-associated neurodegeneration
- Mitochondrial membrane protein-associated neurodegeneration
- Hereditary spastic paraplegia
- COASY protein-associated neurodegeneration
- Beta-propeller protein-associated neurodegeneration
- Leukodystrophy
Zentrum für angeborene pädiatrische Stoffwechselerkrankungen am LMU Klinikum München
Care for Rare Center am Dr. von Haunerschen Kinderspital am LMU Klinikum München LMU Klinikum München Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum
Lindwurmstr. 4
80337 München
- Very long chain acyl-CoA dehydrogenase deficiency
- Disorder of urea cycle metabolism and ammonia detoxification
- Phenylketonuria
- Glycogen storage disease
- Medium chain acyl-CoA dehydrogenase deficiency
- Mitochondrial disease
- Tyrosinemia type 1
- Galactosemia
- Glutaryl-CoA dehydrogenase deficiency
- Fabry disease
- Maple syrup urine disease
- Disorder of carnitine cycle and carnitine transport
Zentrum für mitochondriale Erkrankungen am LMU Klinikum München
Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum LMU Klinikum München
Ziemssenstraße 1
80336 München
089 440057400
089 440057402
Website
Email
- MERRF
- Mitochondrial DNA depletion syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Barth syndrome
- Mitochondrial myopathy
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Recessive mitochondrial ataxia syndrome
- Kearns-Sayre syndrome
- Coenzyme Q10 deficiency
- MELAS
- Maternally-inherited diabetes and deafness
- Leber hereditary optic neuropathy
- Mitochondrial neurogastrointestinal encephalomyopathy
- Pearson syndrome
Klinik für Kinder- und Jugendmedizin Reutlingen
Steinenbergstrasse 31
72764 Reutlingen
071 212004051
071 212004481
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