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