Low lying larynx
We report a rare case of laryngotracheal anomaly and its possible etiology and mode of presentation. A teenager presented with voice change and a neck lump. Investigations revealed a laryngeal anomaly in which the larynx was hyperdescended. It was accompanied by low lying thyroid gland and hyoid bon...
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my.um.eprints.124292015-01-28T03:30:04Z http://eprints.um.edu.my/12429/ Low lying larynx Govindaraju, R. Rajagopalan, R. Omar, R. Mukari, S.A.M. Q Science (General) We report a rare case of laryngotracheal anomaly and its possible etiology and mode of presentation. A teenager presented with voice change and a neck lump. Investigations revealed a laryngeal anomaly in which the larynx was hyperdescended. It was accompanied by low lying thyroid gland and hyoid bone together with an absence of a cervical segment of the esophagus and trachea. The anomaly only became noticeable secondary to pubertal changes in the thyroid cartilage of the teenager. An embryological defect during the formation of the laryngotracheal tube and esophagus is a possible explanation of this anomaly. The present case probably represents the third reported of its kind. Blackwell Publishing 2010 Article PeerReviewed Govindaraju, R. and Rajagopalan, R. and Omar, R. and Mukari, S.A.M. (2010) Low lying larynx. Congenital Anomalies, 50 (3). pp. 193-196. |
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Q Science (General) Govindaraju, R. Rajagopalan, R. Omar, R. Mukari, S.A.M. Low lying larynx |
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We report a rare case of laryngotracheal anomaly and its possible etiology and mode of presentation. A teenager presented with voice change and a neck lump. Investigations revealed a laryngeal anomaly in which the larynx was hyperdescended. It was accompanied by low lying thyroid gland and hyoid bone together with an absence of a cervical segment of the esophagus and trachea. The anomaly only became noticeable secondary to pubertal changes in the thyroid cartilage of the teenager. An embryological defect during the formation of the laryngotracheal tube and esophagus is a possible explanation of this anomaly. The present case probably represents the third reported of its kind. |
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Article |
author |
Govindaraju, R. Rajagopalan, R. Omar, R. Mukari, S.A.M. |
author_facet |
Govindaraju, R. Rajagopalan, R. Omar, R. Mukari, S.A.M. |
author_sort |
Govindaraju, R. |
title |
Low lying larynx |
title_short |
Low lying larynx |
title_full |
Low lying larynx |
title_fullStr |
Low lying larynx |
title_full_unstemmed |
Low lying larynx |
title_sort |
low lying larynx |
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Blackwell Publishing |
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2010 |
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http://eprints.um.edu.my/12429/ |
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1643689295918137344 |
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13.160551 |