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17p11.2 Google OMIM PubMed Who named it? [Charcot-Marie-Tooth disease] Charcot-Marie-Tooth disease, demyelinating, type 1A *Gene map locus 17p11.2 CMT1A Charcot-Marie-Tooth Neuropathy, type 1A Charcot-Marie-Tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1A Charcot-Marie-Tooth disease, slow nerve conduction type, unlinked to Duffy HMSN1A Hereditary motor and sensory neuropathy IA [Clinical features: decreased motor nerve conduction velocity; segmental demyelination and remyelination with onion bulb formations on nerve biopsy] [Inheritance: autosomal dominant] |
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Coexistent hereditary and inflammatory neuropathy |
Coexistent hereditary and inflammatory neuropathy |
Coexistent hereditary and inflammatory neuropathy |
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Brain |
Brain |
Brain |
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Edited by Aldo Campana,
August 21, 2012
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