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