Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation
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MGZ Medizinisch Genetisches Zentrum München
Bayerstr. 3-5
80335 München
089 30908860
089 309088666
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Universitäts NeuroMuskuläres Centrum am Universitätsklinikum Dresden
UniversitätsCentrum für Seltene Erkrankungen Dresden (USE) Universitätsklinikum Carl Gustav Carus Dresden
Fetscherstr. 74
01307 Dresden
0351 4583876
0351 4585802
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- Amyotrophic lateral sclerosis
- Myotonic dystrophy
- Juvenile myasthenia gravis
- Duchenne and Becker muscular dystrophy
- Dermatomyositis
- Botulism
- Malignant hyperthermia of anesthesia
- Charcot-Marie-Tooth disease type 1
- Rhabdomyosarcoma
- Limb-girdle muscular dystrophy
- Guillain-Barré syndrome
- Lambert-Eaton myasthenic syndrome
Zentrum für neuromuskuläre Erkrankungen im Kindesalter am Universitätsklinikum Freiburg
Universitätsklinikum Freiburg Freiburg Zentrum für Seltene Erkrankungen (FZSE)
Mathildenstraße 1
79106 Freiburg
- Microcephaly-complex motor and sensory axonal neuropathy syndrome
- Emery-Dreifuss muscular dystrophy
- Becker muscular dystrophy
- Limb-girdle muscular dystrophy
- Spinocerebellar ataxia with axonal neuropathy type 1
- Duchenne muscular dystrophy
- Proximal spinal muscular atrophy
- Bulbospinal muscular atrophy
- Muscular dystrophy
- Autosomal dominant slowed nerve conduction velocity
- Motor neuron disease
- Distal hereditary motor neuropathy type 1
- Distal myopathy
- Amyotrophic lateral sclerosis
- Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome