Keratosis Palmoplantaris Striata Iii; Ppks3

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Alternative names

Keratosis Palmoplantaris Striata Iii; Ppks3 Is also known as kpps3, keratoderma, palmoplantar, striate form iii, striate palmoplantar keratoderma iii, sppk3.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Keratosis Palmoplantaris Striata Iii; Ppks3 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
KRT1. By Institute for Human Genetics University Clinic Freiburg (Germany). KRT1 Specificity 100 % Genes 100 %
KRT1. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). KRT1 Specificity 100 % Genes 100 %
KRT1. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). KRT1 Specificity 100 % Genes 100 %
KRT1. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). KRT1 Specificity 100 % Genes 100 %
KRT1. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). KRT1 Specificity 100 % Genes 100 %
Epidermolytic hyperkeratosis (sequence analysis of KRT1 gene). By CGC Genetics (Portugal). KRT1 Specificity 100 % Genes 100 %
Epidermolysis bullosa (NGS panel for 18 genes). By CGC Genetics (Portugal). DST, FERMT1, COL17A1, COL7A1, DSP, EXPH5, ITGA3, ITGA6, ITGB4, KRT1, KRT10, KRT14, KRT5, LAMA3, LAMB3, LAMC2, MMP1, PLEC Specificity 6 % Genes 100 %
Congenital Ichthyosis and Related Disorders Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). SLC27A4, ST14, TGM1, ALOXE3, ABCA12, CLDN1, POMP, PNPLA1, ABHD5, LIPN, CERS3, CYP4F22, NIPAL4, ALOX12B, AP1S1, KRT1, KRT10, KRT2, KRT9 Specificity 6 % Genes 100 %

Sources and references

You can check the following sources for additional information.

OMIM MESH Rare Disease Search Engine

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