cervical spine instability
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H-INDEX

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2021 ◽  
Vol 9 (33) ◽  
pp. 10369-10373
Author(s):  
Ce Zhu ◽  
Hui-Liang Yang ◽  
Gi Hye Im ◽  
Li-Min Liu ◽  
Chun-Guang Zhou ◽  
...  

2020 ◽  
Vol 11 (5) ◽  
pp. 876-882
Author(s):  
Husham A. Al-daoseri ◽  
Mubder A. Mohammed Saeed ◽  
Rafal A. Ahmed

Genes ◽  
2019 ◽  
Vol 10 (10) ◽  
pp. 764 ◽  
Author(s):  
Camerota ◽  
Ritelli ◽  
Wischmeijer ◽  
Majore ◽  
Cinquina ◽  
...  

Loeys-Dietz syndrome (LDS) is a connective tissue disorder first described in 2005 featuring aortic/arterial aneurysms, dissections, and tortuosity associated with craniofacial, osteoarticular, musculoskeletal, and cutaneous manifestations. Heterozygous mutations in 6 genes (TGFBR1/2, TGFB2/3, SMAD2/3), encoding components of the TGF-β pathway, cause LDS. Such genetic heterogeneity mirrors broad phenotypic variability with significant differences, especially in terms of the age of onset, penetrance, and severity of life-threatening vascular manifestations and multiorgan involvement, indicating the need to obtain genotype-to-phenotype correlations for personalized management and counseling. Herein, we report on a cohort of 34 LDS patients from 24 families all receiving a molecular diagnosis. Fifteen variants were novel, affecting the TGFBR1 (6), TGFBR2 (6), SMAD3 (2), and TGFB2 (1) genes. Clinical features were scored for each distinct gene and matched with literature data to strengthen genotype-phenotype correlations such as more severe vascular manifestations in TGFBR1/2-related LDS. Additional features included spontaneous pneumothorax in SMAD3-related LDS and cervical spine instability in TGFB2-related LDS. Our study broadens the clinical and molecular spectrum of LDS and indicates that a phenotypic continuum emerges as more patients are described, although genotype-phenotype correlations may still contribute to clinical management.


2019 ◽  
Vol 28 (2) ◽  
pp. 183-7
Author(s):  
Mohamad Saekhu ◽  
Samsul Ashari ◽  
David Tandian ◽  
Setyo Widi Nugroho

Bicycle mishap, a common and ordinary event occurring in children, can have devastating consequences associated with cervical spine injury. Furthermore, either diagnosis or surgical management of cervical spine injury in children is a challenging issue. This research report a challenging case of an anterior cervical corpectomy and fusion with plating in a 7-year-old boy due to cervical spine instability with spinal cord compression after a bicycle mishap. After 20 months of the primary surgery, the titanium-based cervical plate was removed by a second surgery to allow the growth of the cervical spine.


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