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Atrichia with Papular Lesions
Atrichia with papular lesions (APL) is a rare autosomal recessive form of irreversible alopecia with onset at few months of age with papular keratin cysts over the body. It is associated with mutation in the Zinc finger domain of the human hairless gene on chromosome region 8p12. An eleven-year-old...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250007/ https://www.ncbi.nlm.nih.gov/pubmed/22223974 http://dx.doi.org/10.4103/0974-7753.90827 |
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author | Bansal, Manish Manchanda, Kajal Lamba, Sachin Pandey, SS |
author_facet | Bansal, Manish Manchanda, Kajal Lamba, Sachin Pandey, SS |
author_sort | Bansal, Manish |
collection | PubMed |
description | Atrichia with papular lesions (APL) is a rare autosomal recessive form of irreversible alopecia with onset at few months of age with papular keratin cysts over the body. It is associated with mutation in the Zinc finger domain of the human hairless gene on chromosome region 8p12. An eleven-year-old male presented with extensive alopecia starting at six months of age refractory to the treatment along with keratotic papules on the face and trunk. Biopsy from a papule showed mid-dermal keratin cysts and from the scalp showed few vellus follicles with no terminal hairs. The diagnosis of APL was made based upon the criteria proposed. Vitamin D-dependent rickets was ruled out as it has similar clinical presentation. Accurate diagnosis of APL is required to avoid unnecessary treatment to the patient as it is commonly misdiagnosed as alopecia universalis and treated with systemic steroids. |
format | Online Article Text |
id | pubmed-3250007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-32500072012-01-05 Atrichia with Papular Lesions Bansal, Manish Manchanda, Kajal Lamba, Sachin Pandey, SS Int J Trichology Case Report Atrichia with papular lesions (APL) is a rare autosomal recessive form of irreversible alopecia with onset at few months of age with papular keratin cysts over the body. It is associated with mutation in the Zinc finger domain of the human hairless gene on chromosome region 8p12. An eleven-year-old male presented with extensive alopecia starting at six months of age refractory to the treatment along with keratotic papules on the face and trunk. Biopsy from a papule showed mid-dermal keratin cysts and from the scalp showed few vellus follicles with no terminal hairs. The diagnosis of APL was made based upon the criteria proposed. Vitamin D-dependent rickets was ruled out as it has similar clinical presentation. Accurate diagnosis of APL is required to avoid unnecessary treatment to the patient as it is commonly misdiagnosed as alopecia universalis and treated with systemic steroids. Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC3250007/ /pubmed/22223974 http://dx.doi.org/10.4103/0974-7753.90827 Text en Copyright: © International Journal of Trichology 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Bansal, Manish Manchanda, Kajal Lamba, Sachin Pandey, SS Atrichia with Papular Lesions |
title | Atrichia with Papular Lesions |
title_full | Atrichia with Papular Lesions |
title_fullStr | Atrichia with Papular Lesions |
title_full_unstemmed | Atrichia with Papular Lesions |
title_short | Atrichia with Papular Lesions |
title_sort | atrichia with papular lesions |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250007/ https://www.ncbi.nlm.nih.gov/pubmed/22223974 http://dx.doi.org/10.4103/0974-7753.90827 |
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