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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Main Authors: Govindaraju, R., Rajagopalan, R., Omar, R., Mukari, S.A.M.
Format: Article
Published: Blackwell Publishing 2010
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Online Access:http://eprints.um.edu.my/12429/
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spelling 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.
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic Q Science (General)
spellingShingle Q Science (General)
Govindaraju, R.
Rajagopalan, R.
Omar, R.
Mukari, S.A.M.
Low lying larynx
description 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.
format 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
publisher Blackwell Publishing
publishDate 2010
url http://eprints.um.edu.my/12429/
_version_ 1643689295918137344
score 13.160551