GENETIC PATTERN, ORTHODONTIC AND SURGICAL MANAGEMENT OF MULTIPLE SUPPLEMENTARY IMPACTED TEETH IN A RARE, CLEIDOCRANIAL DYSPLASIA PATIENT: A CASE REPORT

Background: Cleidocranial dysplasia (CCD) is a rare, autosomal dominant skeletal dysplasia with a prevalence of one per million births.The main causes of CCD are mutations in the core-binding factor alpha-1 (CBFA1) or runt-related transcription factor-2 (RUNX2), located at the 6p21 chromosomal region.RUNX2 plays important roles in osteoblast differ

Observational studies based on cohorts built from electronic 24" Barstool health records (EHR) form the backbone of our current understanding of the risk of new-onset diabetes following COVID.EHR-based research is a powerful tool for medical research but is subject to multiple sources of bias.In this viewpoint, Cable Covers we define key sources of

Children are the most vulnerable groups in society, and their adult standing is profoundly influenced by their formative experiences, mindset, and quality of interactions.The aim of the current research is to investigate the lived experiences of the childhood of imprisoned women and its continuation in their current situation.This research is a qua

Since the approval for the treatment of melanoma in 2014, immune checkpoint inhibitors (ICIs) Neutral Cleaner have revolutionized the therapy pattern across various malignancies.Coinciding with their frequent usage, their adverse effects, including fever, cannot be neglected.In the context of cancer diseases and cancer treatments, fever of unknown