Atlantoaxial dislocation in the setting of NMLFS

IF 1.6 4区 医学 Q3 GENETICS & HEREDITY European journal of medical genetics Pub Date : 2024-06-01 DOI:10.1016/j.ejmg.2024.104947
Yousaf Abughofah , Andrew J. Witten , Ahmed Belal , Saul Wilson
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Abstract

Background

Nablus mask-like facial syndrome (NMFLS) is an extremely rare genetic syndrome characterized by facial dysmorphia as well as developmental delay. In the present report we describe a potential association between non-traumatic atlanto-occipital dislocation and NMFLS in an 11-year old female lacking typical facial features of NMFLS.

Case description

An 11-year-old female with autism presented with symptoms of persistent headache and vomiting as well as neck stiffness. Further investigation and CT imaging revealed congenital malformation of the skull base and craniocervical junction with complete posterior subluxation of the left occipital condyle. MRI findings later corroborated the findings on CT.

Conclusions

The patient was successfully treated with occipitocervical fusion. The findings in this case suggest the possibility that atlanto-occipital instability and generalized occipitocervical may be associated with NMFLS.

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寰椎脱位与 NMLFS。
背景:纳布卢斯面具样面部综合征(NMFLS)是一种极为罕见的遗传综合征,其特征是面部畸形和发育迟缓。在本报告中,我们描述了一名 11 岁女性非外伤性寰枕脱位与 NMFLS 之间的潜在关联:一名患有自闭症的 11 岁女性出现了持续性头痛、呕吐和颈部僵硬的症状。进一步检查和 CT 成像显示她的颅底和颅颈交界处有先天性畸形,左枕骨髁完全后脱位。核磁共振成像结果后来证实了 CT 的结果:该患者成功接受了枕颈融合术。本病例的研究结果表明,寰枕不稳和全身性枕颈可能与 NMFLS 有关。
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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
193
审稿时长
66 days
期刊介绍: The European Journal of Medical Genetics (EJMG) is a peer-reviewed journal that publishes articles in English on various aspects of human and medical genetics and of the genetics of experimental models. Original clinical and experimental research articles, short clinical reports, review articles and letters to the editor are welcome on topics such as : • Dysmorphology and syndrome delineation • Molecular genetics and molecular cytogenetics of inherited disorders • Clinical applications of genomics and nextgen sequencing technologies • Syndromal cancer genetics • Behavioral genetics • Community genetics • Fetal pathology and prenatal diagnosis • Genetic counseling.
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