Cargando…

Mal de Meleda with Congenital Cataract: A Novel Case Report

Mal de meleda (MdM), a rare autosomal recessive genodermatosis is characterized by erythema and hyperkeratosis of the palms and soles with a sharp demarcation and that progress with age (progrediens) and extend to the dorsal aspects of the hands and feet (transgrediens). It has been associated with...

Descripción completa

Detalles Bibliográficos
Autores principales: Sethi, Anisha, Janda, Jaspreet Kaur, Sharma, Nidhi, Malhotra, SK
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4601461/
https://www.ncbi.nlm.nih.gov/pubmed/26538740
http://dx.doi.org/10.4103/0019-5154.159655
_version_ 1782394556493332480
author Sethi, Anisha
Janda, Jaspreet Kaur
Sharma, Nidhi
Malhotra, SK
author_facet Sethi, Anisha
Janda, Jaspreet Kaur
Sharma, Nidhi
Malhotra, SK
author_sort Sethi, Anisha
collection PubMed
description Mal de meleda (MdM), a rare autosomal recessive genodermatosis is characterized by erythema and hyperkeratosis of the palms and soles with a sharp demarcation and that progress with age (progrediens) and extend to the dorsal aspects of the hands and feet (transgrediens). It has been associated with various conditions albeit rarely with congenial cataract. Ocular lens and the skin have the same embryological origins. We hereby present this novel case report of Mal de meleda in association with congenital posterior subcapsular cataract which to the best of our knowledge has not been reported from India before.
format Online
Article
Text
id pubmed-4601461
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-46014612015-11-04 Mal de Meleda with Congenital Cataract: A Novel Case Report Sethi, Anisha Janda, Jaspreet Kaur Sharma, Nidhi Malhotra, SK Indian J Dermatol E-IJD Case Report Mal de meleda (MdM), a rare autosomal recessive genodermatosis is characterized by erythema and hyperkeratosis of the palms and soles with a sharp demarcation and that progress with age (progrediens) and extend to the dorsal aspects of the hands and feet (transgrediens). It has been associated with various conditions albeit rarely with congenial cataract. Ocular lens and the skin have the same embryological origins. We hereby present this novel case report of Mal de meleda in association with congenital posterior subcapsular cataract which to the best of our knowledge has not been reported from India before. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4601461/ /pubmed/26538740 http://dx.doi.org/10.4103/0019-5154.159655 Text en Copyright: © Indian Journal of Dermatology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle E-IJD Case Report
Sethi, Anisha
Janda, Jaspreet Kaur
Sharma, Nidhi
Malhotra, SK
Mal de Meleda with Congenital Cataract: A Novel Case Report
title Mal de Meleda with Congenital Cataract: A Novel Case Report
title_full Mal de Meleda with Congenital Cataract: A Novel Case Report
title_fullStr Mal de Meleda with Congenital Cataract: A Novel Case Report
title_full_unstemmed Mal de Meleda with Congenital Cataract: A Novel Case Report
title_short Mal de Meleda with Congenital Cataract: A Novel Case Report
title_sort mal de meleda with congenital cataract: a novel case report
topic E-IJD Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4601461/
https://www.ncbi.nlm.nih.gov/pubmed/26538740
http://dx.doi.org/10.4103/0019-5154.159655
work_keys_str_mv AT sethianisha maldemeledawithcongenitalcataractanovelcasereport
AT jandajaspreetkaur maldemeledawithcongenitalcataractanovelcasereport
AT sharmanidhi maldemeledawithcongenitalcataractanovelcasereport
AT malhotrask maldemeledawithcongenitalcataractanovelcasereport