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http://dx.doi.org/10.1097/01.brs.0000240410.06755.63 | DOI Listing |
Acta Neurochir (Wien)
November 2024
Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Spine (Phila Pa 1976)
November 2024
Cohen Children's Medical Center, Department of Pediatric Orthopaedics, New Hyde Park, NY.
Eur J Pediatr
September 2024
Division of Pediatric Genetics, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
Achondroplasia (ACH; MIM #100,800), caused by a heterozygous gain of function pathogenic variant in the fibroblast growth factor receptor 3 gene (FGFR3; MIM*134,934), is the most prevalent and most readily identifiable cause of disproportionate short stature that is compatible with life. In addition, individuals with achondroplasia face significant medical, functional, and psychosocial challenges throughout their lives. This study assessed associated morbidities in patients with achondroplasia at a single center in Turkey.
View Article and Find Full Text PDFExp Ther Med
June 2024
Department of Orthopaedics, Beijing Friendship Hospital Pinggu Campus, Capital Medical University, Beijing 101200, P.R. China.
The pathogenesis of adolescent idiopathic scoliosis (AIS) remains unclear. It has been found that interleukin-6 (IL-6) rs1800795 locus and matrix metalloproteinase-3 (MMP-3) rs3025058 locus gene polymorphisms may be associated with AIS susceptibility, which has been controversial and needs to be further confirmed by updated meta-analysis. The aim of the present study was to investigate the association of MMP-3 rs3025058 and IL-6 rs1800795 single nucleotide polymorphisms (SNPs) with susceptibility to AIS.
View Article and Find Full Text PDFIran J Public Health
January 2024
Department of Health & Sport Rehabilitation, Faculty of Sport Science & Health, University of Shahid Beheshti, Tehran, Iran.
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