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Coexistence of Ankylosing Spondylitis and Neurofibromatosis Type 1
Ankylosing spondylitis (AS) is a systemic disease primarily characterized by the inflammation of sacroiliac joints and axial skeleton. Neurofibromatosis type 1 (NF1) is a multisystem genetic disease which is characterized by cutaneous findings, most importantly café-au-lait spots and axillary freckl...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5002286/ https://www.ncbi.nlm.nih.gov/pubmed/27597922 http://dx.doi.org/10.1155/2016/4039801 |
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author | Gundogdu, Baris Yolbas, Servet Yildirim, Ahmet Gonen, Murat Koca, Suleyman Serdar |
author_facet | Gundogdu, Baris Yolbas, Servet Yildirim, Ahmet Gonen, Murat Koca, Suleyman Serdar |
author_sort | Gundogdu, Baris |
collection | PubMed |
description | Ankylosing spondylitis (AS) is a systemic disease primarily characterized by the inflammation of sacroiliac joints and axial skeleton. Neurofibromatosis type 1 (NF1) is a multisystem genetic disease which is characterized by cutaneous findings, most importantly café-au-lait spots and axillary freckling, by skeletal dysplasia, and by the growth of both benign and malignant nervous system neoplasms, most notably benign neurofibromas. In this case report, we present a 43-year-old male with AS and NF1. |
format | Online Article Text |
id | pubmed-5002286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-50022862016-09-05 Coexistence of Ankylosing Spondylitis and Neurofibromatosis Type 1 Gundogdu, Baris Yolbas, Servet Yildirim, Ahmet Gonen, Murat Koca, Suleyman Serdar Case Rep Rheumatol Case Report Ankylosing spondylitis (AS) is a systemic disease primarily characterized by the inflammation of sacroiliac joints and axial skeleton. Neurofibromatosis type 1 (NF1) is a multisystem genetic disease which is characterized by cutaneous findings, most importantly café-au-lait spots and axillary freckling, by skeletal dysplasia, and by the growth of both benign and malignant nervous system neoplasms, most notably benign neurofibromas. In this case report, we present a 43-year-old male with AS and NF1. Hindawi Publishing Corporation 2016 2016-08-14 /pmc/articles/PMC5002286/ /pubmed/27597922 http://dx.doi.org/10.1155/2016/4039801 Text en Copyright © 2016 Baris Gundogdu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Gundogdu, Baris Yolbas, Servet Yildirim, Ahmet Gonen, Murat Koca, Suleyman Serdar Coexistence of Ankylosing Spondylitis and Neurofibromatosis Type 1 |
title | Coexistence of Ankylosing Spondylitis and Neurofibromatosis Type 1 |
title_full | Coexistence of Ankylosing Spondylitis and Neurofibromatosis Type 1 |
title_fullStr | Coexistence of Ankylosing Spondylitis and Neurofibromatosis Type 1 |
title_full_unstemmed | Coexistence of Ankylosing Spondylitis and Neurofibromatosis Type 1 |
title_short | Coexistence of Ankylosing Spondylitis and Neurofibromatosis Type 1 |
title_sort | coexistence of ankylosing spondylitis and neurofibromatosis type 1 |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5002286/ https://www.ncbi.nlm.nih.gov/pubmed/27597922 http://dx.doi.org/10.1155/2016/4039801 |
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