Mitochondrial membrane protein-associated neurodegeneration
All Entries 4
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
- Recessive mitochondrial ataxia syndrome
- Leber hereditary optic neuropathy
- Coenzyme Q10 deficiency
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Mitochondrial DNA depletion syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Kearns-Sayre syndrome
- Mitochondrial neurogastrointestinal encephalomyopathy
- Maternally-inherited diabetes and deafness
- MERRF
- Pearson syndrome
- Barth syndrome
- Mitochondrial myopathy
- MELAS
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
- Infantile neuroaxonal dystrophy
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Hereditary spastic paraplegia
- Leukodystrophy
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Classic pantothenate kinase-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Mitochondrial disease
- Neuroferritinopathy
- Atypical pantothenate kinase-associated neurodegeneration
- Rare ataxia
Institut für Humangenetik am Klinikums rechts der Isar der Technischen Universität München
Klinikum rechts der Isar der Technischen Universität München
Trogerstr. 32
81675 München
089 41406381
089 41406382
Website
Email
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Fatty acid hydroxylase-associated neurodegeneration
- Aceruloplasminemia
- Woodhouse-Sakati syndrome
- Infantile neuroaxonal dystrophy
- Adult-onset dystonia-parkinsonism
- PLA2G6-associated neurodegeneration
- Kufor-Rakeb syndrome
- Neuroferritinopathy
- Neurodegeneration with brain iron accumulation
- COASY protein-associated neurodegeneration
- Autosomal recessive spastic paraplegia type 35
- Pantothenate kinase-associated neurodegeneration
- Beta-propeller protein-associated neurodegeneration
Parent facilities 0
Genetic Advices 1
Institut für Humangenetik am Klinikums rechts der Isar der Technischen Universität München
Klinikum rechts der Isar der Technischen Universität München
Trogerstr. 32
81675 München
089 41406381
089 41406382
Website
Email
Care facilities 2
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
- Recessive mitochondrial ataxia syndrome
- Leber hereditary optic neuropathy
- Coenzyme Q10 deficiency
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Mitochondrial DNA depletion syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Kearns-Sayre syndrome
- Mitochondrial neurogastrointestinal encephalomyopathy
- Maternally-inherited diabetes and deafness
- MERRF
- Pearson syndrome
- Barth syndrome
- Mitochondrial myopathy
- MELAS
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
- Infantile neuroaxonal dystrophy
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Hereditary spastic paraplegia
- Leukodystrophy
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Classic pantothenate kinase-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Mitochondrial disease
- Neuroferritinopathy
- Atypical pantothenate kinase-associated neurodegeneration
- Rare ataxia
Supportgroups 1
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Fatty acid hydroxylase-associated neurodegeneration
- Aceruloplasminemia
- Woodhouse-Sakati syndrome
- Infantile neuroaxonal dystrophy
- Adult-onset dystonia-parkinsonism
- PLA2G6-associated neurodegeneration
- Kufor-Rakeb syndrome
- Neuroferritinopathy
- Neurodegeneration with brain iron accumulation
- COASY protein-associated neurodegeneration
- Autosomal recessive spastic paraplegia type 35
- Pantothenate kinase-associated neurodegeneration
- Beta-propeller protein-associated neurodegeneration