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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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Formato: | Texto |
Lenguaje: | English |
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Medknow Publications
2009
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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. |
format | Text |
id | pubmed-2876703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
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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