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Primary Ciliary Dyskinesia and Situs Ambiguus: A Rare Association

Primary ciliary dyskinesia (PCD) is a rare disorder with impaired ciliary function resulting in a spectrum of clinical manifestations of varying severity. PCD affects approximately one in every 20,000 individuals with a reported prevalence between 1:4000 and 1:50,000. Due to its nonspecific clinical...

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Autores principales: Narahari, Kumar Narahari, Kapoor, Anu, Sanamandra, Sarat Kumar, Varma Gunturi, Surya Ramachandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5846221/
https://www.ncbi.nlm.nih.gov/pubmed/29552537
http://dx.doi.org/10.4103/ijabmr.IJABMR_341_16
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author Narahari, Kumar Narahari
Kapoor, Anu
Sanamandra, Sarat Kumar
Varma Gunturi, Surya Ramachandra
author_facet Narahari, Kumar Narahari
Kapoor, Anu
Sanamandra, Sarat Kumar
Varma Gunturi, Surya Ramachandra
author_sort Narahari, Kumar Narahari
collection PubMed
description Primary ciliary dyskinesia (PCD) is a rare disorder with impaired ciliary function resulting in a spectrum of clinical manifestations of varying severity. PCD affects approximately one in every 20,000 individuals with a reported prevalence between 1:4000 and 1:50,000. Due to its nonspecific clinical features, the condition is usually diagnosed late in its course, unless situs inversus (SI) or organ laterality defects are discovered at imaging. A small subset of patients with PCD display associated organ laterality defects, different from the classical SI totalis. We present here, the clinical and imaging findings in a young female with PCD along with left-sided isomerism, a variant of heterotaxy syndromes.
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spelling pubmed-58462212018-03-16 Primary Ciliary Dyskinesia and Situs Ambiguus: A Rare Association Narahari, Kumar Narahari Kapoor, Anu Sanamandra, Sarat Kumar Varma Gunturi, Surya Ramachandra Int J Appl Basic Med Res Case Report Primary ciliary dyskinesia (PCD) is a rare disorder with impaired ciliary function resulting in a spectrum of clinical manifestations of varying severity. PCD affects approximately one in every 20,000 individuals with a reported prevalence between 1:4000 and 1:50,000. Due to its nonspecific clinical features, the condition is usually diagnosed late in its course, unless situs inversus (SI) or organ laterality defects are discovered at imaging. A small subset of patients with PCD display associated organ laterality defects, different from the classical SI totalis. We present here, the clinical and imaging findings in a young female with PCD along with left-sided isomerism, a variant of heterotaxy syndromes. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5846221/ /pubmed/29552537 http://dx.doi.org/10.4103/ijabmr.IJABMR_341_16 Text en Copyright: © 2018 International Journal of Applied and Basic Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Narahari, Kumar Narahari
Kapoor, Anu
Sanamandra, Sarat Kumar
Varma Gunturi, Surya Ramachandra
Primary Ciliary Dyskinesia and Situs Ambiguus: A Rare Association
title Primary Ciliary Dyskinesia and Situs Ambiguus: A Rare Association
title_full Primary Ciliary Dyskinesia and Situs Ambiguus: A Rare Association
title_fullStr Primary Ciliary Dyskinesia and Situs Ambiguus: A Rare Association
title_full_unstemmed Primary Ciliary Dyskinesia and Situs Ambiguus: A Rare Association
title_short Primary Ciliary Dyskinesia and Situs Ambiguus: A Rare Association
title_sort primary ciliary dyskinesia and situs ambiguus: a rare association
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5846221/
https://www.ncbi.nlm.nih.gov/pubmed/29552537
http://dx.doi.org/10.4103/ijabmr.IJABMR_341_16
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