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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
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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.
Pediatric Dermatology
|June 6, 2025
Summary
Researchers identified a new NIPAL4 gene variant causing a rare skin disorder. This finding expands the understanding of the ichthyosis phenotype in children.
Area of Science:
- Genetics
- Dermatology
- Molecular Biology
Background:
- Ichthyosis is a group of genetic skin disorders characterized by dry, scaling skin.
- The NIPAL4 gene is implicated in lipid metabolism and skin barrier function.
- Mutations in NIPAL4 have been associated with ichthyosis, but novel variants continue to be discovered.
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