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