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A 60-year-old Brazilian man gave a 20-year history of progressive bilateral facial weakness. He was known to have lattice corneal dystrophy. His father, two paternal uncles and a son had similar neurological problems. His father was born in Portugal and his paternal grandmother was born in Finland. On examination, there was severe bilateral facial weakness (figure 1). Neurophysiology studies found bilateral axonal facial neuropathy but …
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