Acrokeratosis Verruciformis Of Hopf

Description

Acrokeratosis verruciformis of Hopf is a localized disorder of keratinization affecting the distal extremities. Onset occurs early in life (Dhitavat et al., 2003).

Clinical Features

Phenotypes and symptoms related to Acrokeratosis Verruciformis Of Hopf

  • Hyperkeratosis
  • Epidermal acanthosis
  • Ridged nail
  • Subungual hyperkeratosis
  • Acrokeratosis

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

Acrokeratosis Verruciformis Of Hopf Is also known as akv of hopf, hopf disease.

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.


Mendelian

Accelerate your rare disease diagnosis with us

Learn more

Acrokeratosis Verruciformis Of Hopf Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Epilepsy Advanced Sequencing and CNV Evaluation.

By Athena Diagnostics Inc (United States).

SCN1A, SCN1B, SCN2A, SCN3A, SCN5A, SCN8A, SCN9A, SHH, ST3GAL3, ST3GAL5, STIL, SIX3, SLC2A1, SLC35A2, SLC6A1, SLC6A8, SLC9A6, SMC1A, KDM5C, SMS , (...)

View the complete list with 214 more genes
Specificity
1 %
Genes
100 %
Epilepsy Advanced Sequencing and CNV Evaluation - Syndromic Disorders.

By Athena Diagnostics Inc (United States).

SYNGAP1, TBX1, TSC1, TSC2, SETBP1, PANK2, ADGRV1, ATP6V0A2, MAGI2, VPS13A, ANKRD11, VPS13B, KIF1BP, KANSL1, SMC3, PIGV, NIPBL, ROGDI, GFAP, HPRT1 , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
100 %
ATP2A2.

By Institute for Human Genetics University Clinic Freiburg (Germany).

ATP2A2
Specificity
100 %
Genes
100 %
ATP2A2 Gene Sequencing.

By GeneDx (United States).

ATP2A2
Specificity
100 %
Genes
100 %
ATP2A2. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).

ATP2A2
Specificity
100 %
Genes
100 %
Darier disease (sequence analysis of ATP2A2 gene).

By CGC Genetics (Portugal).

ATP2A2
Specificity
100 %
Genes
100 %
Darier-White disease (deletion/duplication analysis on ATP2A2 gene).

By CGC Genetics (Portugal).

ATP2A2
Specificity
100 %
Genes
100 %
Darier-White disease (deletion/duplication analysis on ATP2A2 gene).

By CGC Genetics (Portugal).

ATP2A2
Specificity
100 %
Genes
100 %

We have 13 more panels available in our App

Get the app

Sources and references

You can check the following sources for additional information.

OMIM ORPHANET Rare Disease Search Engine

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like TIBIAL HEMIMELIA FECHTNER SYNDROME; FTNS KLEEFSTRA SYNDROME 2; KLEFS2 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A; CMT1A

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more