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Description
Diagnostics and treatments evolve as new information and experience is acquired
Concern: Dullness, dark spots, uneven tone
BMC Res
Epub 2013 Jul 31
Conversely, autosomal dominant mutations (classified as CMT2K) generally present a milder, later-onset phenotype, characterized by slowly progressing distal weakness and sensory loss, with maintained ambulation into adulthood [32]
