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Monogenic hypertension

Hypertension is a significant public health problem. Thirty percent of cases are caused by a single genetic mutation. Hypertension is the predominant and usually the only manifestation in monogenic hypertension Monogenic hypertension may involve mineralcorticoid-dependent or -independent increase in...

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Autores principales: Precone, Vincenza, Krasi, Geraldo, Guerri, Giulia, Stuppia, Liborio, Romeo, Francesco, Perrone, Marco, Marinelli, Carla, Zulian, Alessandra, Dallavilla, Tiziano, Bertelli, Matteo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7233634/
https://www.ncbi.nlm.nih.gov/pubmed/31577254
http://dx.doi.org/10.23750/abm.v90i10-S.8759
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author Precone, Vincenza
Krasi, Geraldo
Guerri, Giulia
Stuppia, Liborio
Romeo, Francesco
Perrone, Marco
Marinelli, Carla
Zulian, Alessandra
Dallavilla, Tiziano
Bertelli, Matteo
author_facet Precone, Vincenza
Krasi, Geraldo
Guerri, Giulia
Stuppia, Liborio
Romeo, Francesco
Perrone, Marco
Marinelli, Carla
Zulian, Alessandra
Dallavilla, Tiziano
Bertelli, Matteo
author_sort Precone, Vincenza
collection PubMed
description Hypertension is a significant public health problem. Thirty percent of cases are caused by a single genetic mutation. Hypertension is the predominant and usually the only manifestation in monogenic hypertension Monogenic hypertension may involve mineralcorticoid-dependent or -independent increase in Na(+) transport. Diagnosis is based on routine physical examination, blood pressure measurement and laboratory analysis of renin, aldosterone, cortisol and potassium. Genetic testing is useful for confirming diagnosis and for differential diagnosis. Monogenic hypertension has autosomal dominant or autosomal recessive inheritance. (www.actabiomedica.it)
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spelling pubmed-72336342020-05-19 Monogenic hypertension Precone, Vincenza Krasi, Geraldo Guerri, Giulia Stuppia, Liborio Romeo, Francesco Perrone, Marco Marinelli, Carla Zulian, Alessandra Dallavilla, Tiziano Bertelli, Matteo Acta Biomed Review Hypertension is a significant public health problem. Thirty percent of cases are caused by a single genetic mutation. Hypertension is the predominant and usually the only manifestation in monogenic hypertension Monogenic hypertension may involve mineralcorticoid-dependent or -independent increase in Na(+) transport. Diagnosis is based on routine physical examination, blood pressure measurement and laboratory analysis of renin, aldosterone, cortisol and potassium. Genetic testing is useful for confirming diagnosis and for differential diagnosis. Monogenic hypertension has autosomal dominant or autosomal recessive inheritance. (www.actabiomedica.it) Mattioli 1885 2019 2019-09-30 /pmc/articles/PMC7233634/ /pubmed/31577254 http://dx.doi.org/10.23750/abm.v90i10-S.8759 Text en Copyright: © 2019 ACTA BIO MEDICA SOCIETY OF MEDICINE AND NATURAL SCIENCES OF PARMA http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution 4.0 International License
spellingShingle Review
Precone, Vincenza
Krasi, Geraldo
Guerri, Giulia
Stuppia, Liborio
Romeo, Francesco
Perrone, Marco
Marinelli, Carla
Zulian, Alessandra
Dallavilla, Tiziano
Bertelli, Matteo
Monogenic hypertension
title Monogenic hypertension
title_full Monogenic hypertension
title_fullStr Monogenic hypertension
title_full_unstemmed Monogenic hypertension
title_short Monogenic hypertension
title_sort monogenic hypertension
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7233634/
https://www.ncbi.nlm.nih.gov/pubmed/31577254
http://dx.doi.org/10.23750/abm.v90i10-S.8759
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