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Rare complications of neurofibromatosis 1 diagnosed incidentally in two children
Neurofibromatosis 1 (NF1) is an autosomal-dominant disorder with various clinical expressivity and complications. Arterial hypertension may be present in patients with NF1 and is secondary to vasculopathy or pheochromocytoma. We herein describe two children (17 and 4 years old) diagnosed late with N...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6124468/ https://www.ncbi.nlm.nih.gov/pubmed/30214218 http://dx.doi.org/10.2147/TCRM.S173237 |
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author | Lazea, Cecilia Asavoaie, Carmen Al-Khzouz, Camelia Popa, Lenuta |
author_facet | Lazea, Cecilia Asavoaie, Carmen Al-Khzouz, Camelia Popa, Lenuta |
author_sort | Lazea, Cecilia |
collection | PubMed |
description | Neurofibromatosis 1 (NF1) is an autosomal-dominant disorder with various clinical expressivity and complications. Arterial hypertension may be present in patients with NF1 and is secondary to vasculopathy or pheochromocytoma. We herein describe two children (17 and 4 years old) diagnosed late with NF1 after severe arterial hypertension had been discovered due to pheochromocytoma and middle aortic syndrome. Routine measurement of arterial pressure is mandatory in children with NF1, in order to diagnose the complications of this disease. |
format | Online Article Text |
id | pubmed-6124468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61244682018-09-13 Rare complications of neurofibromatosis 1 diagnosed incidentally in two children Lazea, Cecilia Asavoaie, Carmen Al-Khzouz, Camelia Popa, Lenuta Ther Clin Risk Manag Case Series Neurofibromatosis 1 (NF1) is an autosomal-dominant disorder with various clinical expressivity and complications. Arterial hypertension may be present in patients with NF1 and is secondary to vasculopathy or pheochromocytoma. We herein describe two children (17 and 4 years old) diagnosed late with NF1 after severe arterial hypertension had been discovered due to pheochromocytoma and middle aortic syndrome. Routine measurement of arterial pressure is mandatory in children with NF1, in order to diagnose the complications of this disease. Dove Medical Press 2018-08-31 /pmc/articles/PMC6124468/ /pubmed/30214218 http://dx.doi.org/10.2147/TCRM.S173237 Text en © 2018 Lazea et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Case Series Lazea, Cecilia Asavoaie, Carmen Al-Khzouz, Camelia Popa, Lenuta Rare complications of neurofibromatosis 1 diagnosed incidentally in two children |
title | Rare complications of neurofibromatosis 1 diagnosed incidentally in two children |
title_full | Rare complications of neurofibromatosis 1 diagnosed incidentally in two children |
title_fullStr | Rare complications of neurofibromatosis 1 diagnosed incidentally in two children |
title_full_unstemmed | Rare complications of neurofibromatosis 1 diagnosed incidentally in two children |
title_short | Rare complications of neurofibromatosis 1 diagnosed incidentally in two children |
title_sort | rare complications of neurofibromatosis 1 diagnosed incidentally in two children |
topic | Case Series |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6124468/ https://www.ncbi.nlm.nih.gov/pubmed/30214218 http://dx.doi.org/10.2147/TCRM.S173237 |
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