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
Ziemssenstraße 1
80336 München
089 440057400
089 440057402
Website
Email
- Maternally-inherited diabetes and deafness
- MERRF
- Kearns-Sayre syndrome
- Mitochondrial DNA depletion syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Mitochondrial myopathy
- Barth syndrome
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Recessive mitochondrial ataxia syndrome
- Coenzyme Q10 deficiency
- MELAS
- Pearson syndrome
- Leber hereditary optic neuropathy
- Mitochondrial neurogastrointestinal encephalomyopathy
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057470
089 440057402
Website
Email
- Atypical pantothenate kinase-associated neurodegeneration
- Leukodystrophy
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial membrane protein-associated neurodegeneration
- Hereditary spastic paraplegia
- Myasthenia gravis
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Rare ataxia
- Beta-propeller protein-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- COASY protein-associated neurodegeneration
- Neuroferritinopathy
- Mitochondrial disease
- Neurodegeneration with brain iron accumulation
Institut für Humangenetik am TUM Klinikum Rechts der Isar
TUM Klinikum Rechts der Isar
Trogerstr. 32
81675 München
089 41406381
089 41406382
Website
Email
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Kufor-Rakeb syndrome
- Neurodegeneration with brain iron accumulation
- Neuroferritinopathy
- Aceruloplasminemia
- PLA2G6-associated neurodegeneration
- Adult-onset dystonia-parkinsonism
- Woodhouse-Sakati syndrome
- Infantile neuroaxonal dystrophy
- Fatty acid hydroxylase-associated neurodegeneration
- Autosomal recessive spastic paraplegia type 35
- COASY protein-associated neurodegeneration
- Beta-propeller protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
Parent facilities 0
Genetic Advices 1
Institut für Humangenetik am TUM Klinikum Rechts der Isar
TUM Klinikum Rechts der Isar
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
Ziemssenstraße 1
80336 München
089 440057400
089 440057402
Website
Email
- Maternally-inherited diabetes and deafness
- MERRF
- Kearns-Sayre syndrome
- Mitochondrial DNA depletion syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Mitochondrial myopathy
- Barth syndrome
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Recessive mitochondrial ataxia syndrome
- Coenzyme Q10 deficiency
- MELAS
- Pearson syndrome
- Leber hereditary optic neuropathy
- Mitochondrial neurogastrointestinal encephalomyopathy
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057470
089 440057402
Website
Email
- Atypical pantothenate kinase-associated neurodegeneration
- Leukodystrophy
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial membrane protein-associated neurodegeneration
- Hereditary spastic paraplegia
- Myasthenia gravis
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Rare ataxia
- Beta-propeller protein-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- COASY protein-associated neurodegeneration
- Neuroferritinopathy
- Mitochondrial disease
- Neurodegeneration with brain iron accumulation
Supportgroups 1
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Kufor-Rakeb syndrome
- Neurodegeneration with brain iron accumulation
- Neuroferritinopathy
- Aceruloplasminemia
- PLA2G6-associated neurodegeneration
- Adult-onset dystonia-parkinsonism
- Woodhouse-Sakati syndrome
- Infantile neuroaxonal dystrophy
- Fatty acid hydroxylase-associated neurodegeneration
- Autosomal recessive spastic paraplegia type 35
- COASY protein-associated neurodegeneration
- Beta-propeller protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration