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Kartagener's syndrome: A case series

Kartagener's syndrome is a rare, autosomal recessive genetic ciliary disorder comprising the triad of situs inversus, chronic sinusitis, and bronchiectasis. The basic problem lies in the defective movement of cilia, leading to recurrent chest infections, ear/nose/throat symptoms, and infertilit...

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Autores principales: Mishra, Mayank, Kumar, Naresh, Jaiswal, Ashish, Verma, Ajay K., Kant, Surya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519024/
https://www.ncbi.nlm.nih.gov/pubmed/23243352
http://dx.doi.org/10.4103/0970-2113.102831
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author Mishra, Mayank
Kumar, Naresh
Jaiswal, Ashish
Verma, Ajay K.
Kant, Surya
author_facet Mishra, Mayank
Kumar, Naresh
Jaiswal, Ashish
Verma, Ajay K.
Kant, Surya
author_sort Mishra, Mayank
collection PubMed
description Kartagener's syndrome is a rare, autosomal recessive genetic ciliary disorder comprising the triad of situs inversus, chronic sinusitis, and bronchiectasis. The basic problem lies in the defective movement of cilia, leading to recurrent chest infections, ear/nose/throat symptoms, and infertility. We hereby report three unusual cases of this rare entity – an infertile male with azoospermia in whom Bochdalek's diaphragmatic hernia coexisted, another case of an infertile female, and a third of an infertile male with oligospermia. The need for a high index of suspicion to make an early diagnosis cannot be overemphasized in such patients so that wherever possible, options for timely treatment of infertility may be offered and unnecessary evaluation of symptoms is avoided.
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spelling pubmed-35190242012-12-14 Kartagener's syndrome: A case series Mishra, Mayank Kumar, Naresh Jaiswal, Ashish Verma, Ajay K. Kant, Surya Lung India Case Report Kartagener's syndrome is a rare, autosomal recessive genetic ciliary disorder comprising the triad of situs inversus, chronic sinusitis, and bronchiectasis. The basic problem lies in the defective movement of cilia, leading to recurrent chest infections, ear/nose/throat symptoms, and infertility. We hereby report three unusual cases of this rare entity – an infertile male with azoospermia in whom Bochdalek's diaphragmatic hernia coexisted, another case of an infertile female, and a third of an infertile male with oligospermia. The need for a high index of suspicion to make an early diagnosis cannot be overemphasized in such patients so that wherever possible, options for timely treatment of infertility may be offered and unnecessary evaluation of symptoms is avoided. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3519024/ /pubmed/23243352 http://dx.doi.org/10.4103/0970-2113.102831 Text en Copyright: © Lung India 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Mishra, Mayank
Kumar, Naresh
Jaiswal, Ashish
Verma, Ajay K.
Kant, Surya
Kartagener's syndrome: A case series
title Kartagener's syndrome: A case series
title_full Kartagener's syndrome: A case series
title_fullStr Kartagener's syndrome: A case series
title_full_unstemmed Kartagener's syndrome: A case series
title_short Kartagener's syndrome: A case series
title_sort kartagener's syndrome: a case series
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519024/
https://www.ncbi.nlm.nih.gov/pubmed/23243352
http://dx.doi.org/10.4103/0970-2113.102831
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