Erythrokeratodermia Variabilis due to a Compound Heterozygous Variants in the NIPAL4 Gene

Luis Fernando Sánchez-Espino1,2, Marta Ivars3, Asunción Vicente-López3

  • 1Dermatology Division, Pediatrics Department, Stollery Children's Hospital, Edmonton, Alberta, Canada.

PubMed
Summary

Researchers identified a new NIPAL4 gene variant causing a rare skin disorder. This finding expands the understanding of the ichthyosis phenotype in children.

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