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