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Adolescent Congenital Central Hypoventilation Syndrome: An Easily Overlooked Diagnosis
Congenital central hypoventilation syndrome (CCHS), also known as Ondine’s curse, is a rare, potentially fatal genetic disease, manifesting as a lack of respiratory drive. Most diagnoses are made in pediatric patients, however late-onset cases have been rarely reported. Due to the milder symptoms at...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8703802/ https://www.ncbi.nlm.nih.gov/pubmed/34949014 http://dx.doi.org/10.3390/ijerph182413402 |
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author | Ditmer, Marta Turkiewicz, Szymon Gabryelska, Agata Sochal, Marcin Białasiewicz, Piotr |
author_facet | Ditmer, Marta Turkiewicz, Szymon Gabryelska, Agata Sochal, Marcin Białasiewicz, Piotr |
author_sort | Ditmer, Marta |
collection | PubMed |
description | Congenital central hypoventilation syndrome (CCHS), also known as Ondine’s curse, is a rare, potentially fatal genetic disease, manifesting as a lack of respiratory drive. Most diagnoses are made in pediatric patients, however late-onset cases have been rarely reported. Due to the milder symptoms at presentation that might easily go overlooked, these late-onset cases can result in serious health consequences later in life. Here, we present a case report of late-onset CCHS in an adolescent female patient. In this review we summarize the current knowledge about symptoms, as well as clinical management of CCHS, and describe in detail the molecular mechanism responsible for this disorder. |
format | Online Article Text |
id | pubmed-8703802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87038022021-12-25 Adolescent Congenital Central Hypoventilation Syndrome: An Easily Overlooked Diagnosis Ditmer, Marta Turkiewicz, Szymon Gabryelska, Agata Sochal, Marcin Białasiewicz, Piotr Int J Environ Res Public Health Review Congenital central hypoventilation syndrome (CCHS), also known as Ondine’s curse, is a rare, potentially fatal genetic disease, manifesting as a lack of respiratory drive. Most diagnoses are made in pediatric patients, however late-onset cases have been rarely reported. Due to the milder symptoms at presentation that might easily go overlooked, these late-onset cases can result in serious health consequences later in life. Here, we present a case report of late-onset CCHS in an adolescent female patient. In this review we summarize the current knowledge about symptoms, as well as clinical management of CCHS, and describe in detail the molecular mechanism responsible for this disorder. MDPI 2021-12-20 /pmc/articles/PMC8703802/ /pubmed/34949014 http://dx.doi.org/10.3390/ijerph182413402 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Ditmer, Marta Turkiewicz, Szymon Gabryelska, Agata Sochal, Marcin Białasiewicz, Piotr Adolescent Congenital Central Hypoventilation Syndrome: An Easily Overlooked Diagnosis |
title | Adolescent Congenital Central Hypoventilation Syndrome: An Easily Overlooked Diagnosis |
title_full | Adolescent Congenital Central Hypoventilation Syndrome: An Easily Overlooked Diagnosis |
title_fullStr | Adolescent Congenital Central Hypoventilation Syndrome: An Easily Overlooked Diagnosis |
title_full_unstemmed | Adolescent Congenital Central Hypoventilation Syndrome: An Easily Overlooked Diagnosis |
title_short | Adolescent Congenital Central Hypoventilation Syndrome: An Easily Overlooked Diagnosis |
title_sort | adolescent congenital central hypoventilation syndrome: an easily overlooked diagnosis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8703802/ https://www.ncbi.nlm.nih.gov/pubmed/34949014 http://dx.doi.org/10.3390/ijerph182413402 |
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