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