Palmoplantar keratoderma: An unusual manifestation of hypohydrotic ectodermic dysplasia

Rapp–Hodgkin syndrome (RHS) is a rare condition that is characterized by ectodermal dysplasia and palatal abnormalities. Palmoplantar keratoderma (PPK) is an unusual manifestation of hidrotic ED. Ulcerations on the palms are also not common in RHS. We describe a 15‐year‐old boy who has RHS associate...

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Autores principales: Abdelli, Wissal, Souissi, Asmahen, Alaoui, Fatima, Sassi, Wiem, Chelly, Ines, Haouat, Slim, Mokni, Mourad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918462/
https://www.ncbi.nlm.nih.gov/pubmed/35310322
http://dx.doi.org/10.1002/ccr3.5577
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author Abdelli, Wissal
Souissi, Asmahen
Alaoui, Fatima
Sassi, Wiem
Chelly, Ines
Haouat, Slim
Mokni, Mourad
author_facet Abdelli, Wissal
Souissi, Asmahen
Alaoui, Fatima
Sassi, Wiem
Chelly, Ines
Haouat, Slim
Mokni, Mourad
author_sort Abdelli, Wissal
collection PubMed
description Rapp–Hodgkin syndrome (RHS) is a rare condition that is characterized by ectodermal dysplasia and palatal abnormalities. Palmoplantar keratoderma (PPK) is an unusual manifestation of hidrotic ED. Ulcerations on the palms are also not common in RHS. We describe a 15‐year‐old boy who has RHS associated with PPK.
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spelling pubmed-89184622022-03-18 Palmoplantar keratoderma: An unusual manifestation of hypohydrotic ectodermic dysplasia Abdelli, Wissal Souissi, Asmahen Alaoui, Fatima Sassi, Wiem Chelly, Ines Haouat, Slim Mokni, Mourad Clin Case Rep Case Reports Rapp–Hodgkin syndrome (RHS) is a rare condition that is characterized by ectodermal dysplasia and palatal abnormalities. Palmoplantar keratoderma (PPK) is an unusual manifestation of hidrotic ED. Ulcerations on the palms are also not common in RHS. We describe a 15‐year‐old boy who has RHS associated with PPK. John Wiley and Sons Inc. 2022-03-13 /pmc/articles/PMC8918462/ /pubmed/35310322 http://dx.doi.org/10.1002/ccr3.5577 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Reports
Abdelli, Wissal
Souissi, Asmahen
Alaoui, Fatima
Sassi, Wiem
Chelly, Ines
Haouat, Slim
Mokni, Mourad
Palmoplantar keratoderma: An unusual manifestation of hypohydrotic ectodermic dysplasia
title Palmoplantar keratoderma: An unusual manifestation of hypohydrotic ectodermic dysplasia
title_full Palmoplantar keratoderma: An unusual manifestation of hypohydrotic ectodermic dysplasia
title_fullStr Palmoplantar keratoderma: An unusual manifestation of hypohydrotic ectodermic dysplasia
title_full_unstemmed Palmoplantar keratoderma: An unusual manifestation of hypohydrotic ectodermic dysplasia
title_short Palmoplantar keratoderma: An unusual manifestation of hypohydrotic ectodermic dysplasia
title_sort palmoplantar keratoderma: an unusual manifestation of hypohydrotic ectodermic dysplasia
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918462/
https://www.ncbi.nlm.nih.gov/pubmed/35310322
http://dx.doi.org/10.1002/ccr3.5577
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