書誌事項
- タイトル別名
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- A Case of Waardenburg's Syndrome Type I Found through Unilateral Hearing Loss
- 臨床 一側性の難聴で発見されたWaardenburg症候群1型例
- リンショウ イッソクセイ ノ ナンチョウ デ ハッケン サレタ Waardenburg ショウコウグン 1ガタレイ
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Waardenburg’s syndrome is a hereditary disease which shows lateral displacement of the inner canthi, broad nasal root, hyperplasia of the eyebrows, albinism of the frontal head hair, congenital hearing loss, and heterochromia iridis. This syndrome is classified into 4 types by its presenting symptoms. We reported a case of Waardenburg’s syndrome type I. The patient was a 6-month-old male with left side hearing loss, heterochromia iridis, lateral displacement of the inner canthi, hyperplasia of the eyebrows. Since the characteristic features are important information to diagnose this syndrome, it is important to pay attention to the features of patients complaining of congenital hearing loss.<br>
収録刊行物
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- 耳鼻咽喉科臨床
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耳鼻咽喉科臨床 103 (2), 121-124, 2010
耳鼻咽喉科臨床学会
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詳細情報 詳細情報について
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- CRID
- 1390282679239410432
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- NII論文ID
- 10026216563
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- NII書誌ID
- AN00107089
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- ISSN
- 18844545
- 00326313
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- NDL書誌ID
- 10579119
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- 本文言語コード
- ja
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- データソース種別
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- JaLC
- NDL
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