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