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An unusual presentation of immotile-cilia syndrome with azoospermia: Case report and literature review

Immotile-cilia syndrome is a rare disorder characterized by chronic recurrent sino-pulmonary infection, impaired tracheobronchial clearance, situs inversus in about 50% of cases, and living but immotile spermatozoa of normal morphology in semen analysis. In this report, we describe an unusual presen...

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Detalles Bibliográficos
Autores principales: Dixit, Ramakant, Dixit, Kalpana, Jindal, Savita, Shah, K. V.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2876703/
https://www.ncbi.nlm.nih.gov/pubmed/20532000
http://dx.doi.org/10.4103/0970-2113.56352
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author Dixit, Ramakant
Dixit, Kalpana
Jindal, Savita
Shah, K. V.
author_facet Dixit, Ramakant
Dixit, Kalpana
Jindal, Savita
Shah, K. V.
author_sort Dixit, Ramakant
collection PubMed
description Immotile-cilia syndrome is a rare disorder characterized by chronic recurrent sino-pulmonary infection, impaired tracheobronchial clearance, situs inversus in about 50% of cases, and living but immotile spermatozoa of normal morphology in semen analysis. In this report, we describe an unusual presentation of immotile-cilia syndrome with azoospermia in a 32-year-old male patient. The diagnosis was based on history of recurrent respiratory tract infection, bronchiectasis, maxillary sinusitis, hypoplasia of frontal sinuses, dextrocardia with situs inversus, impaired nasal mucociliary clearance, etc. Semen analysis revealed azoospermia without any evidence of obstruction in epididymides or vas deference. Normal spermatogenesis was seen on testicular biopsy.
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spelling pubmed-28767032010-06-08 An unusual presentation of immotile-cilia syndrome with azoospermia: Case report and literature review Dixit, Ramakant Dixit, Kalpana Jindal, Savita Shah, K. V. Lung India Case Report Immotile-cilia syndrome is a rare disorder characterized by chronic recurrent sino-pulmonary infection, impaired tracheobronchial clearance, situs inversus in about 50% of cases, and living but immotile spermatozoa of normal morphology in semen analysis. In this report, we describe an unusual presentation of immotile-cilia syndrome with azoospermia in a 32-year-old male patient. The diagnosis was based on history of recurrent respiratory tract infection, bronchiectasis, maxillary sinusitis, hypoplasia of frontal sinuses, dextrocardia with situs inversus, impaired nasal mucociliary clearance, etc. Semen analysis revealed azoospermia without any evidence of obstruction in epididymides or vas deference. Normal spermatogenesis was seen on testicular biopsy. Medknow Publications 2009 /pmc/articles/PMC2876703/ /pubmed/20532000 http://dx.doi.org/10.4103/0970-2113.56352 Text en © Lung India http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Dixit, Ramakant
Dixit, Kalpana
Jindal, Savita
Shah, K. V.
An unusual presentation of immotile-cilia syndrome with azoospermia: Case report and literature review
title An unusual presentation of immotile-cilia syndrome with azoospermia: Case report and literature review
title_full An unusual presentation of immotile-cilia syndrome with azoospermia: Case report and literature review
title_fullStr An unusual presentation of immotile-cilia syndrome with azoospermia: Case report and literature review
title_full_unstemmed An unusual presentation of immotile-cilia syndrome with azoospermia: Case report and literature review
title_short An unusual presentation of immotile-cilia syndrome with azoospermia: Case report and literature review
title_sort unusual presentation of immotile-cilia syndrome with azoospermia: case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2876703/
https://www.ncbi.nlm.nih.gov/pubmed/20532000
http://dx.doi.org/10.4103/0970-2113.56352
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