Syndrome d'anomalies congénitales multiples-hypotonie-épilepsie type 2
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Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
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089 440057402
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- Mitochondrial disease
- Neuroferritinopathy
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Rare ataxia
- Neurodegeneration with brain iron accumulation
- Infantile neuroaxonal dystrophy
- Hereditary spastic paraplegia
- Leukodystrophy
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Myasthenia gravis
- Atypical pantothenate kinase-associated neurodegeneration
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial membrane protein-associated neurodegeneration