PA11: A Rare Case of Severe Papulopustular Dermatosis Secondary to a Germline EGFR Mutation
June 2026
in “
British Journal of Dermatology
”
Studysummary In this case report, researchers observed a Slovakian neonate with a rare EGFR genetic mutation who presented with severe neonatal dermatoses, ichthyosis, and multisystem complications, emphasizing the significance of genetic diagnosis for such complex conditions.
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