Keratosis Palmoplantaris Striata Iii; Ppks3

Clinical Features

Phenotypes and symptoms related to Keratosis Palmoplantaris Striata Iii; Ppks3

  • Palmoplantar keratoderma

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 %

You can get up to 23 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM MESH Rare Disease Search Engine

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