Cargando…

A case of haemoptysis in a girl with Noonan syndrome

Noonan syndrome (NS) is an autosomal dominant condition affecting 1 in 2 000 live births. It is characterised by distinctive physical features, congenital heart disease and multiple other comorbidities including haematological abnormalities. Haemoptysis is the expectoration of blood originating from...

Descripción completa

Detalles Bibliográficos
Autores principales: Mopeli, R K, Lebea, M, Verwey, C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: South African Medical Association 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8203073/
https://www.ncbi.nlm.nih.gov/pubmed/34240029
http://dx.doi.org/10.7196/AJTCCM.2020.v26i3.023
_version_ 1783708092393848832
author Mopeli, R K
Lebea, M
Verwey, C
author_facet Mopeli, R K
Lebea, M
Verwey, C
author_sort Mopeli, R K
collection PubMed
description Noonan syndrome (NS) is an autosomal dominant condition affecting 1 in 2 000 live births. It is characterised by distinctive physical features, congenital heart disease and multiple other comorbidities including haematological abnormalities. Haemoptysis is the expectoration of blood originating from the lower respiratory tract. It is uncommon in children but can be life threatening.Perfusion of the lower respiratory system arises from the pulmonary arterial circulation and the bronchial circulation, or bleeding may arise from either. In children, the most common causes of haemoptysis are respiratory tract infections, aspirated foreign bodies and bronchiectasis. We present a 7-year-old girl with recurrent haemoptysis.
format Online
Article
Text
id pubmed-8203073
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher South African Medical Association
record_format MEDLINE/PubMed
spelling pubmed-82030732021-07-07 A case of haemoptysis in a girl with Noonan syndrome Mopeli, R K Lebea, M Verwey, C Afr J Thorac Crit Care Med Case Report Noonan syndrome (NS) is an autosomal dominant condition affecting 1 in 2 000 live births. It is characterised by distinctive physical features, congenital heart disease and multiple other comorbidities including haematological abnormalities. Haemoptysis is the expectoration of blood originating from the lower respiratory tract. It is uncommon in children but can be life threatening.Perfusion of the lower respiratory system arises from the pulmonary arterial circulation and the bronchial circulation, or bleeding may arise from either. In children, the most common causes of haemoptysis are respiratory tract infections, aspirated foreign bodies and bronchiectasis. We present a 7-year-old girl with recurrent haemoptysis. South African Medical Association 2020-10-13 /pmc/articles/PMC8203073/ /pubmed/34240029 http://dx.doi.org/10.7196/AJTCCM.2020.v26i3.023 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution - NonCommercial Works License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Mopeli, R K
Lebea, M
Verwey, C
A case of haemoptysis in a girl with Noonan syndrome
title A case of haemoptysis in a girl with Noonan syndrome
title_full A case of haemoptysis in a girl with Noonan syndrome
title_fullStr A case of haemoptysis in a girl with Noonan syndrome
title_full_unstemmed A case of haemoptysis in a girl with Noonan syndrome
title_short A case of haemoptysis in a girl with Noonan syndrome
title_sort case of haemoptysis in a girl with noonan syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8203073/
https://www.ncbi.nlm.nih.gov/pubmed/34240029
http://dx.doi.org/10.7196/AJTCCM.2020.v26i3.023
work_keys_str_mv AT mopelirk acaseofhaemoptysisinagirlwithnoonansyndrome
AT lebeam acaseofhaemoptysisinagirlwithnoonansyndrome
AT verweyc acaseofhaemoptysisinagirlwithnoonansyndrome
AT mopelirk caseofhaemoptysisinagirlwithnoonansyndrome
AT lebeam caseofhaemoptysisinagirlwithnoonansyndrome
AT verweyc caseofhaemoptysisinagirlwithnoonansyndrome