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