Mitochondrial membrane protein-associated neurodegeneration
All Entries 4
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
Website
Email
- Mitochondrial disease
- Neuroferritinopathy
- Neurodegeneration with brain iron accumulation
- Huntington disease
- Pantothenate kinase-associated neurodegeneration
- Leukodystrophy
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Hereditary spastic paraplegia
- Mitochondrial membrane protein-associated neurodegeneration
- Rare ataxia
- Atypical pantothenate kinase-associated neurodegeneration
- Classic pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
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
- MERRF
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Mitochondrial neurogastrointestinal encephalomyopathy
- Pearson syndrome
- Mitochondrial DNA depletion syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Maternally-inherited diabetes and deafness
- Kearns-Sayre syndrome
- Coenzyme Q10 deficiency
- Recessive mitochondrial ataxia syndrome
- Leber hereditary optic neuropathy
- MELAS
- Barth syndrome
- Mitochondrial myopathy
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
- Infantile neuroaxonal dystrophy
- Woodhouse-Sakati syndrome
- Fatty acid hydroxylase-associated neurodegeneration
- Autosomal recessive spastic paraplegia type 35
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Kufor-Rakeb syndrome
- Neurodegeneration with brain iron accumulation
- Aceruloplasminemia
- Neuroferritinopathy
- PLA2G6-associated neurodegeneration
- Adult-onset dystonia-parkinsonism
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
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
Website
Email
- Mitochondrial disease
- Neuroferritinopathy
- Neurodegeneration with brain iron accumulation
- Huntington disease
- Pantothenate kinase-associated neurodegeneration
- Leukodystrophy
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Hereditary spastic paraplegia
- Mitochondrial membrane protein-associated neurodegeneration
- Rare ataxia
- Atypical pantothenate kinase-associated neurodegeneration
- Classic pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
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
- MERRF
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Mitochondrial neurogastrointestinal encephalomyopathy
- Pearson syndrome
- Mitochondrial DNA depletion syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Maternally-inherited diabetes and deafness
- Kearns-Sayre syndrome
- Coenzyme Q10 deficiency
- Recessive mitochondrial ataxia syndrome
- Leber hereditary optic neuropathy
- MELAS
- Barth syndrome
- Mitochondrial myopathy
Supportgroups 1
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Infantile neuroaxonal dystrophy
- Woodhouse-Sakati syndrome
- Fatty acid hydroxylase-associated neurodegeneration
- Autosomal recessive spastic paraplegia type 35
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Kufor-Rakeb syndrome
- Neurodegeneration with brain iron accumulation
- Aceruloplasminemia
- Neuroferritinopathy
- PLA2G6-associated neurodegeneration
- Adult-onset dystonia-parkinsonism