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Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome: A Case Report and Review of Cases Reported from India
Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome is characterized by the triad of follicular keratotic papules, total to subtotal alopecia, and photophobia. We hereby report a case of IFAP syndrome in a 1-year-old boy who presented with all these classical features along with hyper...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859747/ https://www.ncbi.nlm.nih.gov/pubmed/31807449 http://dx.doi.org/10.4103/idoj.IDOJ_19_19 |
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author | Bains, Anupama Vedant, Deepak Verma, Anurag Bhardwaj, Abhishek Nalwa, Aasma |
author_facet | Bains, Anupama Vedant, Deepak Verma, Anurag Bhardwaj, Abhishek Nalwa, Aasma |
author_sort | Bains, Anupama |
collection | PubMed |
description | Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome is characterized by the triad of follicular keratotic papules, total to subtotal alopecia, and photophobia. We hereby report a case of IFAP syndrome in a 1-year-old boy who presented with all these classical features along with hyperkeratotic plaques over knees, plantar keratoderma, and umbilical hernia. Also, literature review of cases reported from India is being presented. |
format | Online Article Text |
id | pubmed-6859747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-68597472019-12-05 Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome: A Case Report and Review of Cases Reported from India Bains, Anupama Vedant, Deepak Verma, Anurag Bhardwaj, Abhishek Nalwa, Aasma Indian Dermatol Online J Case Report Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome is characterized by the triad of follicular keratotic papules, total to subtotal alopecia, and photophobia. We hereby report a case of IFAP syndrome in a 1-year-old boy who presented with all these classical features along with hyperkeratotic plaques over knees, plantar keratoderma, and umbilical hernia. Also, literature review of cases reported from India is being presented. Wolters Kluwer - Medknow 2019-11-01 /pmc/articles/PMC6859747/ /pubmed/31807449 http://dx.doi.org/10.4103/idoj.IDOJ_19_19 Text en Copyright: © 2019 Indian Dermatology Online Journal http://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 Bains, Anupama Vedant, Deepak Verma, Anurag Bhardwaj, Abhishek Nalwa, Aasma Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome: A Case Report and Review of Cases Reported from India |
title | Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome: A Case Report and Review of Cases Reported from India |
title_full | Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome: A Case Report and Review of Cases Reported from India |
title_fullStr | Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome: A Case Report and Review of Cases Reported from India |
title_full_unstemmed | Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome: A Case Report and Review of Cases Reported from India |
title_short | Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome: A Case Report and Review of Cases Reported from India |
title_sort | ichthyosis follicularis, alopecia, and photophobia (ifap) syndrome: a case report and review of cases reported from india |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859747/ https://www.ncbi.nlm.nih.gov/pubmed/31807449 http://dx.doi.org/10.4103/idoj.IDOJ_19_19 |
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