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