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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...

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Autores principales: Lazea, Cecilia, Asavoaie, Carmen, Al-Khzouz, Camelia, Popa, Lenuta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
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.
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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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