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博斯马无鼻小眼综合征(BAMS):来自越南的首例报告。

Bosma Arhinia Microphthalmia Syndrome (BAMS): First Report from Vietnam.

作者信息

Cong Ngo Van, Minh Le Huu Nhat, Hoang Le Huy, Do Uyen, Dung Nguyen Thi My

机构信息

Otolaryngology, Cho Ray Hospital, Ho Chi Minh City, VNM.

College of Medicine, Taipei Medical University, Taipei, TWN.

出版信息

Cureus. 2023 Feb 20;15(2):e35222. doi: 10.7759/cureus.35222. eCollection 2023 Feb.

DOI:10.7759/cureus.35222
PMID:36968924
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10032420/
Abstract

Bosma arhinia microphthalmia syndrome (BAMS) is a rare condition, with about 100 cases identified worldwide. It is characterized by nasal and ophthalmic abnormalities, as well as disturbances in puberty and sexual development. The cardinal sign is arhinia, though some cases have partial aplasia of the external nose. In addition, several reports have revealed abnormal brain structure, including changes to the olfactory bulbs. This case describes a 29-year-old female who has suffered from BAMS since birth. On presentation, she was noted to have congenital arhinia, bilateral microphthalmia, vision loss, mouth-breathing, an unclear speaking voice, a high arched or cleft palate, and a hypoplastic maxilla. Her paranasal sinuses were ossified and underdeveloped. This syndrome occurs rarely, both within Vietnam and worldwide. It is characterized by four major features: arrhinia, complete absence of the paranasal sinuses, eye defects, and absent sexual maturation. This case report describes the presentation of the disorder to improve otolaryngologists' understanding of BAMS. Criteria for diagnosis consist of arhinia, midface hypoplasia (with a hypoplastic maxilla), hypogonadotropic hypogonadism, and normal intellectual abilities. Additional important findings are microphthalmia with or without coloboma, anosmia, maxillary hypoplasia, a high-arched palate, and absence of paranasal sinuses and olfactory bulbs.

摘要

博斯马无鼻小眼综合征(BAMS)是一种罕见疾病,全球确诊病例约100例。其特征为鼻腔和眼部异常,以及青春期和性发育障碍。主要体征是无鼻,不过部分病例存在外鼻部分发育不全。此外,多项报告显示存在脑结构异常,包括嗅球改变。本病例描述了一名自出生就患有BAMS的29岁女性。就诊时,发现她有先天性无鼻、双侧小眼、视力丧失、口呼吸、语音不清、高拱腭或腭裂以及上颌发育不全。她的鼻窦骨化且发育不全。该综合征在越南及全球均很少见。其特征有四个主要方面:无鼻、鼻窦完全缺失、眼部缺陷以及性成熟缺失。本病例报告描述了该疾病的表现,以提高耳鼻喉科医生对BAMS的认识。诊断标准包括无鼻、面中部发育不全(上颌发育不全)、低促性腺激素性性腺功能减退以及智力正常。其他重要发现包括有或无脉络膜缺损的小眼、嗅觉缺失、上颌发育不全、高拱腭以及鼻窦和嗅球缺失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5c6/10032420/7ff6750929d7/cureus-0015-00000035222-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5c6/10032420/4ef23572c964/cureus-0015-00000035222-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5c6/10032420/7ff6750929d7/cureus-0015-00000035222-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5c6/10032420/4ef23572c964/cureus-0015-00000035222-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5c6/10032420/7ff6750929d7/cureus-0015-00000035222-i02.jpg

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本文引用的文献

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2
Twenty-year experience with salvage total laryngectomy: lessons learned.20 年挽救性全喉切除术经验:教训总结。
J Laryngol Otol. 2021 Aug;135(8):729-736. doi: 10.1017/S0022215121001687. Epub 2021 Jul 5.
3
Good Outcome for an Individual with Severe Facial Anomalies and Hypogonadotropic Hypogonadism: A Consequence of His Cognitive Function, Pragmatic Approach, and Temperament.
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Case Rep Pediatr. 2021 Jun 12;2021:9957218. doi: 10.1155/2021/9957218. eCollection 2021.
4
[A Newborn Suffering from Arhinia: Neonatologic Challenges During Primary Care of the Newborn With Bosma Arhinia Microphthalmia Syndrome (BAMS)].[一名患有无鼻症的新生儿:患有博斯马无鼻小眼综合征(BAMS)的新生儿初级护理期间的新生儿学挑战]
Z Geburtshilfe Neonatol. 2020 Dec;224(6):377-380. doi: 10.1055/a-1224-4465. Epub 2020 Sep 3.
5
Bosma arhinia microphthalmia syndrome: Clinical report and review of the literature.博斯马无鼻小眼综合征:临床报告及文献综述
Am J Med Genet A. 2016 May;170A(5):1302-7. doi: 10.1002/ajmg.a.37572. Epub 2016 Feb 3.
6
Bosma arrhinia microphthalmia syndrome in a Mexican patient with a molecular analysis of PAX6.
Clin Dysmorphol. 2016 Jan;25(1):12-5. doi: 10.1097/MCD.0000000000000101.
7
Shape of the dilated aorta in children with bicuspid aortic valve.
Ann Pediatr Cardiol. 2013 Jul;6(2):126-31. doi: 10.4103/0974-2069.115253.
8
Congenital arhinia: A rare case.先天性无鼻:1例罕见病例。
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9
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10
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