[Spastic ectropion of the upper eyelid (apropos of 1 case)].
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Biomedical subjects
Publications and source records attributed to S Morax.
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A report of a family in which three generations were affected by on autosomal dominant corneal dystrophy. The authors studied two fragments of a recurrence on a graft where they noted the presence of granular material. Histochemical studies were negative. Electron microscopy showed the presence of deposits of crystalline appearance resembling those of Groenouw type I dystrophy.
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