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