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