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