C. Cole

M. Zamiri1
J.A. McGrath1
S. Aristodemou1
J.R. McMillan1
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DEAR EDITOR, Loricrin keratoderma (syn. Camisa syndrome, OMIM 604117) is a rare autosomal dominant genodermatosis characterized by palmoplantar keratoderma and ichthyosis. 1,2 It is caused by mutations in loricrin, a small basic protein synthesized in the upper granular layer, which becomes a major constituent of the cornified cell envelope. 3 Seven(More)
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