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. 2010 Apr 21;2010:101452. doi: 10.1155/2010/101452

Table 1.

Published cases of EDSF syndrome with clinical features and observed mutations in PKP 1 gene.

Case1 Clinicopathological findings Observed mutations2 Reference
Epidermal fragility Hyperkeratosis on palms/soles Alopecia Nail dysplasia Hypohidrosis
1 yes yes yes yes yes (a) p.Q304X (b) c.1132ins28 [29]
2 yes yes yes yes yes (a) p.Y71X (b) IVS1−1G>A [31]
3 yes yes yes yes no IVS6−2A>T [32]
4 yes yes yes yes yes IVS11+1G>A [30]
5 yes no yes yes no IVS4−2A>G [33]
6 yes yes yes yes not observed IVS1−1G>A [33]
7 yes yes no yes no IVS9+1G>A [34]
8 yes yes yes yes no (a) c.1053T>A +IVS5+1G>A (b) IVS10−2G>T [35]
9 yes yes yes yes no c.888delC [36]
10 yes yes yes yes not observed p.R672X [37]

1 Numbering of the case correlates to the positions of mutations shown in Figure 2.

2 For compound heterozygosity, mutations of both alleles are given as (a) and (b).