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• Autosomal recessive epidermolysis bullosa simplex due to compound heterozygous mutations in the DST gene: the first Italian case and literature review

  Andrea Diociaiuti, Ruggiero Davide Zingarelli, Dario Francesco D'Urso, Giovanna Zambruno, May El Hachem

  14-05-2025

  https://doi.org/10.4081/dr.2025.10206

  378

  PDF: 283

  HTML: 19
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  Coexistence of reticulate acropigmentation of Kitamura and Dowling-Degos disease

  Ana Rita Cabral, Felicidade Santiago, José Pedro Reis

  e33

  29-09-2011

  https://doi.org/10.4081/dr.2011.e33

  2134

  PDF: 866

  HTML: 4633

• Urbach-Wiethe syndrome: report of two clinical cases

  Ilaria Demofonte, Emanuele Miraglia, Giovanni Pellacani, Sandra Giustini

  20-05-2025

  https://doi.org/10.4081/dr.2025.10230

  395

  PDF: 320

  HTML: 17

• Suspect dyskeratotic neoformations in a 7-year-old child with keratitis-ichthyosis-deafness syndrome: diagnostic, surgical and wound care management

  Alvise Montanari, Francesca Caroppo, Antonio Amabile, Anna Fortina Belloni, Franco Bassetto

  16-04-2024

  https://doi.org/10.4081/dr.2024.9953

  789

  PDF: 511

  HTML: 23
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  Quality of life in Swedish children with congenital ichthyosis

  Agneta Gånemo

  e7

  18-05-2010

  https://doi.org/10.4081/dr.2010.e7

  2184

  PDF: 685

  HTML: 68
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  Focal dermal hypoplasia in a male

  Leni George, Nisha Agrawal, Peter Hogan

  e7

  01-07-2011

  https://doi.org/10.4081/dr.2011.e7

  995

  PDF: 802

  HTML: 170
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  Onychoheterotopia in children

  Marco Ferrari, Vittorio Mazzarello, Egidio Barbi

  05-08-2021

  https://doi.org/10.4081/dr.2021.9068

  2312

  PDF: 488

  HTML: 178

• Papillon-Lefèvre syndrome with excellent response to risankizumab

  Latifah Alibrahim, Sarah Alrashid, Majed Aleissa

  25-02-2026

  https://doi.org/10.4081/dr.2026.10309

  184

  PDF: 182
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  Unilateral Blaschkoid lichen planus in successive pregnancies

  Shiva Kumar, Rajendra Okade, Yasmin Abdul Rahman

  e35

  29-09-2011

  https://doi.org/10.4081/dr.2011.e35

  1539

  PDF: 702

  HTML: 4688