Rare presentation of bilobed posterior tongue in Goldenhar syndrome.

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL BMJ Case Reports Pub Date : 2017-08-01 DOI:10.1136/bcr-2017-219726
Thilaga Rajendran, Ganesh Ramalinggam, Valuyeetham Kamaru Ambu
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引用次数: 6

Abstract

A bilobed posterior tongue is a rare malformation with few reported cases in the literature. This anomaly has not been demonstrated in patients with Goldenhar syndrome. We report a case of a 5-month-old child with the classic signs of Goldenhar syndrome and laryngomalacia with an incidental finding of a bilobed posterior tongue. Careful assessment and monitoring are crucial, especially in syndromic babies.

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戈登哈综合征罕见的双叶后舌表现。
双叶状后舌是一种罕见的畸形,在文献中报道的病例很少。这种异常尚未在Goldenhar综合征患者中得到证实。我们报告一个病例5个月大的孩子与经典迹象的戈登哈综合征和喉软化偶然发现双叶后舌。仔细的评估和监测至关重要,特别是对有综合征的婴儿。
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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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