Two Sisters with Mal de Meleda: Case Series Report

Mal de Meleda (MDM) is a rare autosomal recessive type of palmoplantar keratoderma that is characterized by transgradient keratoderma with scleroatrophy, pseudoainhum around the fingers, and perioral erythema. Its features may also include lichenoid lesions, brachydactyly, and nail dystrophy. The di...

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Autores principales: Cebeci, Dua, Karasel, Seide, Bayraktaroglu, Görgün
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9215182/
https://www.ncbi.nlm.nih.gov/pubmed/35754677
http://dx.doi.org/10.4103/ijabmr.ijabmr_812_21
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author Cebeci, Dua
Karasel, Seide
Bayraktaroglu, Görgün
author_facet Cebeci, Dua
Karasel, Seide
Bayraktaroglu, Görgün
author_sort Cebeci, Dua
collection PubMed
description Mal de Meleda (MDM) is a rare autosomal recessive type of palmoplantar keratoderma that is characterized by transgradient keratoderma with scleroatrophy, pseudoainhum around the fingers, and perioral erythema. Its features may also include lichenoid lesions, brachydactyly, and nail dystrophy. The disease has high morbidity and significantly impairs quality of life. Here, we describe two sisters with typical clinical presentations of MDM and a history of consanguinity between the parents.
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spelling pubmed-92151822022-06-23 Two Sisters with Mal de Meleda: Case Series Report Cebeci, Dua Karasel, Seide Bayraktaroglu, Görgün Int J Appl Basic Med Res Case Report Mal de Meleda (MDM) is a rare autosomal recessive type of palmoplantar keratoderma that is characterized by transgradient keratoderma with scleroatrophy, pseudoainhum around the fingers, and perioral erythema. Its features may also include lichenoid lesions, brachydactyly, and nail dystrophy. The disease has high morbidity and significantly impairs quality of life. Here, we describe two sisters with typical clinical presentations of MDM and a history of consanguinity between the parents. Wolters Kluwer - Medknow 2022 2022-05-10 /pmc/articles/PMC9215182/ /pubmed/35754677 http://dx.doi.org/10.4103/ijabmr.ijabmr_812_21 Text en Copyright: © 2022 International Journal of Applied and Basic Medical Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Cebeci, Dua
Karasel, Seide
Bayraktaroglu, Görgün
Two Sisters with Mal de Meleda: Case Series Report
title Two Sisters with Mal de Meleda: Case Series Report
title_full Two Sisters with Mal de Meleda: Case Series Report
title_fullStr Two Sisters with Mal de Meleda: Case Series Report
title_full_unstemmed Two Sisters with Mal de Meleda: Case Series Report
title_short Two Sisters with Mal de Meleda: Case Series Report
title_sort two sisters with mal de meleda: case series report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9215182/
https://www.ncbi.nlm.nih.gov/pubmed/35754677
http://dx.doi.org/10.4103/ijabmr.ijabmr_812_21
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AT karaselseide twosisterswithmaldemeledacaseseriesreport
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