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. 2015 Jul 23;4:e06322. doi: 10.7554/eLife.06322

Table 1.

Clinical characteristics and genetic causes of 134 index patients with PK

DOI: http://dx.doi.org/10.7554/eLife.06322.012

Genetic causes of 134 index patients with PK
MVK (39*) PMVK (9) MVD (62*) FDPS (4) Unknown (21)
Sex
 Male 27 9 38 1 17
 Female 12 0 24 3 4
Number of lesions
 0–10 4 4 0 0 6
 10–100 20 5 13 0 5
 100–500 5 0 39 0 5
 >500 10 0 10 4 5
Diameter of lesions
 Minimum 2 mm 5 mm 1 mm 1 mm 1 mm
 Maximum 20 cm 5 cm 2 cm 1 cm 2 cm
Age of onset
 At birth 0 0 0 0 3
 0–20 23 4 20 1 0
 20–40 12 3 28 1 9
 40–60 3 1 12 2 5
 >60 1 1 2 0 4
Variants of PK
 DSAP/DSP 26 0 56 4 10
 SFP 0 0 6 0 0
 PM 23 9 0 0 6
 HPM 13 3 1 0 0
 Giant plaque of PPt 19 0 0 0 0
 Genital PK (localized) 0 4 0 0 0
 Porokeratoma 0 5 0 0 0
 LP 1 1 3 0 5
Comorbidity
 Psoriasis vulgaris 4 0 2 0 0
*

One PK patient (proband of family-28, female), who has both the mutation c. 235G>A (MVK) and the mutation c. 746T>C (MVD), was included in both MVK and MVD groups.

The number of lesions is more than 500.

DSAP, disseminated superficial actinic porokeratosis; DSP, disseminated superficial porokeratosis; HPM, hyperkeratotic porokeratosis, LP, linear porokeratosis, PK, porokeratosis; PM, porokeratosis of Mibelli, PPt, porokeratosis ptychotropica; SFP, solar facial porokeratosis.