Complete transverse basilar cleft associated with hemifacial microsomia.

IF 1.4 Q3 ANATOMY & MORPHOLOGY Anatomy & Cell Biology Pub Date : 2024-09-30 Epub Date: 2024-03-07 DOI:10.5115/acb.23.289
Laphatrada Yurasakpong, Athikhun Suwannakhan, Joe Iwanaga, R Shane Tubbs, Arada Chaiyamoon, Nutmethee Kruepunga, Somluk Asuvapongpatana, Thanwa Sudsang
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Abstract

Transverse basilar cleft (TBC) is an extremely rare variation of the clivus or the basilar part of the occipital bone. In this report, a unilateral transverse basilar fissure was found at the clivus in a head computed tomography of an 18-year-old female patient diagnosed with hemifacial microsomia (HFM). Image analysis of this patient showed shortening of the ramus of the right mandible along with medial displacement of the right temporomandibular joint and hypoplastic right maxilla. In addition, observation of the clivus showed a cleft between the basioticum and basioccipital bones at the level of the pharyngeal tubercle on the right side. This cleft was identified as TBC. Clival variations, TBC included, attributed to HFM have never been reported. This report draws attention to the complex relationship between abnormal development of clivus and HFM syndrome, and sheds light on a possible genetic and molecular association between these two conditions.

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伴有半面小畸形的完全横向基底裂。
横基底裂(TBC)是一种极其罕见的枕骨clivus或枕骨基底部分的变异。在本报告中,一名被诊断为半面小畸形(HFM)的 18 岁女性患者在头部计算机断层扫描中发现颅嵴处有单侧横向基底裂。对该患者的图像分析表明,右下颌骨横突缩短,右颞下颌关节向内侧移位,右上颌骨发育不良。此外,对颚骨的观察显示,在右侧咽结节水平的基底骨和枕基骨之间有一个裂隙。该裂隙被鉴定为 TBC。包括 TBC 在内的颅骨变异归因于 HFM 的报道从未有过。本报告提请人们注意颅嵴发育异常与高频综合征之间的复杂关系,并揭示了这两种疾病之间可能存在的遗传和分子关联。
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来源期刊
Anatomy & Cell Biology
Anatomy & Cell Biology ANATOMY & MORPHOLOGY-
CiteScore
1.80
自引率
9.10%
发文量
75
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