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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

  2008

  PDF: 801

  HTML: 4623

• Autosomal recessive epidermolysis bullosa simplex due to compound heterozygous mutations in DST gene: 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

  131

  PDF: 85

• 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

  118

  PDF: 80

• 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

  622

  PDF: 425

  HTML: 15
• 

  Focal dermal hypoplasia in a male

  Leni George, Nisha Agrawal, Peter Hogan

  e7

  01-07-2011

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

  905

  PDF: 736

  HTML: 165
• 

  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

  1428

  PDF: 653

  HTML: 4604
• 

  Quality of life in Swedish children with congenital ichthyosis

  Agneta Gånemo

  e7

  18-05-2010

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

  2033

  PDF: 607

  HTML: 61