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Novel mutations in DSG1 causing striate palmoplantar keratoderma
D Hershkovitz1, J Lugassy, M Indelman
1Department of Dermatology and Laboratory of Molecular Dermatology, Rambam Health Care Campus, Haifa, Israel.
Background:
Striate palmoplantar keratoderma (SPPK) has been shown to be caused by mutations in at least three genes: DSG1, DSP and KRT1.
Methods:
Three families with nine affected members were assessed using a candidate gene-based screening approach.
Results:
In all three families, new heterozygous mutations were found in DSG1.
Conclusion:
Direct sequencing of cDNA derived from affected skin in one patient failed to reveal a pathogenic mutation, suggesting that SPPK results from haploinsufficiency for DSG1.
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