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
- Mitochondrial DNA depletion syndrome
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- MELAS
- MERRF
- Coenzyme Q10 deficiency
- Mitochondrial myopathy
- Barth syndrome
- Kearns-Sayre syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Recessive mitochondrial ataxia syndrome
- Mitochondrial neurogastrointestinal encephalomyopathy
- Pearson syndrome
- Leber hereditary optic neuropathy
- 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
- COASY protein-associated neurodegeneration
- Rare ataxia
- Pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Beta-propeller protein-associated neurodegeneration
- Huntington disease
- Neurodegeneration with brain iron accumulation
- Leukodystrophy
- Atypical pantothenate kinase-associated neurodegeneration
- Hereditary spastic paraplegia
- Mitochondrial disease
- Classic pantothenate kinase-associated neurodegeneration
- Neuroferritinopathy
- Myasthenia gravis
- Mitochondrial membrane protein-associated neurodegeneration
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
- Woodhouse-Sakati syndrome
- Pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- COASY protein-associated neurodegeneration
- Beta-propeller protein-associated neurodegeneration
- PLA2G6-associated neurodegeneration
- Neuroferritinopathy
- Fatty acid hydroxylase-associated neurodegeneration
- Aceruloplasminemia
- Autosomal recessive spastic paraplegia type 35
- Kufor-Rakeb syndrome
- Adult-onset dystonia-parkinsonism
- Neurodegeneration with brain iron accumulation
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
- Mitochondrial DNA depletion syndrome
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- MELAS
- MERRF
- Coenzyme Q10 deficiency
- Mitochondrial myopathy
- Barth syndrome
- Kearns-Sayre syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Recessive mitochondrial ataxia syndrome
- Mitochondrial neurogastrointestinal encephalomyopathy
- Pearson syndrome
- Leber hereditary optic neuropathy
- 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
- COASY protein-associated neurodegeneration
- Rare ataxia
- Pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Beta-propeller protein-associated neurodegeneration
- Huntington disease
- Neurodegeneration with brain iron accumulation
- Leukodystrophy
- Atypical pantothenate kinase-associated neurodegeneration
- Hereditary spastic paraplegia
- Mitochondrial disease
- Classic pantothenate kinase-associated neurodegeneration
- Neuroferritinopathy
- Myasthenia gravis
- Mitochondrial membrane protein-associated neurodegeneration
Supportgroups 1
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Woodhouse-Sakati syndrome
- Pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- COASY protein-associated neurodegeneration
- Beta-propeller protein-associated neurodegeneration
- PLA2G6-associated neurodegeneration
- Neuroferritinopathy
- Fatty acid hydroxylase-associated neurodegeneration
- Aceruloplasminemia
- Autosomal recessive spastic paraplegia type 35
- Kufor-Rakeb syndrome
- Adult-onset dystonia-parkinsonism
- Neurodegeneration with brain iron accumulation