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一名先天性无舌患者的甲状腺功能障碍

Thyroid dysfunction in a patient with aglossia.

作者信息

Kantaputra Piranit, Tanpaiboon Pranoot

机构信息

Department of Pediatric Dentistry, Faculty of Dentistry, Chiang Mai University, Chiang Mai 50200, Thailand.

出版信息

Am J Med Genet A. 2003 Oct 15;122A(3):274-7. doi: 10.1002/ajmg.a.20269.

DOI:10.1002/ajmg.a.20269
PMID:12966532
Abstract

We report a Thai girl who had aglossia, micrognathia, microsomia, collapse of mandibular arch, persistence of buccopharyngeal membrane, microcephaly, and mild developmental delay. Thyroid function tests indicated that she had subclinical hypothyroidism. Thyroid scan revealed normal uptake of the whole thyroid gland. Tongue morphogenesis is integrally linked to the normal development of thyroid gland, and abnormal tongue morphogenesis could potentially result in a functional thyroid disorder. We propose that micrognathia, microsomia, congenital absence of mandibular incisors, and collapse of the mandibular arch are the result of abnormal tongue development.

摘要

我们报告了一名泰国女孩,她患有无舌症、小颌畸形、小身材、下颌弓塌陷、颊咽膜持续存在、小头畸形和轻度发育迟缓。甲状腺功能测试表明她患有亚临床甲状腺功能减退症。甲状腺扫描显示整个甲状腺摄取正常。舌形态发生与甲状腺的正常发育密切相关,异常的舌形态发生可能会导致功能性甲状腺疾病。我们认为小颌畸形、小身材、先天性下颌切牙缺失和下颌弓塌陷是舌发育异常的结果。

相似文献

1
Thyroid dysfunction in a patient with aglossia.一名先天性无舌患者的甲状腺功能障碍
Am J Med Genet A. 2003 Oct 15;122A(3):274-7. doi: 10.1002/ajmg.a.20269.
2
Complete and isolated congenital aglossia: case report and treatment of sequelae using rapid prototyping models.完全性孤立性先天性无舌症:病例报告及使用快速成型模型对后遗症的治疗
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Agnathia (severe micrognathia), aglossia and choanal atresia in an infant.
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A further case of micrognathia, aglossia, and situs inversus totalis with additional features.
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Orthodontic treatment of a patient with hypoglossia.对一名患有舌下功能减退患者的正畸治疗。
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Mandibular symphyseal midline distraction osteogenesis for micrognathia associated with aglossia and situs inversus totalis.
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Congenital aglossia and situs inversus.先天性无舌症与内脏反位。
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Severe congenital hypoglossia and micrognathia with other multiple birth defects.
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The growth of the head of an infant with mandibular micrognathia, glossoptosis and cleft palate following the Beverly Douglas operation.
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Palatomandibular and maxillo-mandibular fusion, partial aglossia and cleft palate in a human embryo. Report of a case.人类胚胎中的腭下颌及上颌下颌融合、部分无舌症和腭裂。一例报告。
Teratology. 1977 Jun;15(3):261-72. doi: 10.1002/tera.1420150308.

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A Rare Clinical Variant of Oromandibular Limb Hypogenesis Syndrome Type I B.I型B型口下颌肢体发育不全综合征的一种罕见临床变异型。
Int J Clin Pediatr Dent. 2016 Jan-Mar;9(1):78-81. doi: 10.5005/jp-journals-10005-1338. Epub 2016 Apr 22.
2
Aglossia: Case Report.无舌症:病例报告。
Int Arch Otorhinolaryngol. 2016 Jan;20(1):87-92. doi: 10.1055/s-0034-1544116. Epub 2015 Jan 30.
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Isolated aglossia in a six year old child presenting with impaired speech: a case report.一名六岁儿童出现言语障碍伴孤立性无舌症:病例报告
Cases J. 2009 Sep 17;2:7926. doi: 10.4076/1757-1626-2-7926.