AI Article Synopsis
- Cleidocranial dysplasia (CCD) is a rare genetic disorder that leads to distinctive skeletal and dental issues, requiring a combination of imaging and clinical assessment for diagnosis.
- The case report focuses on a 25-year-old male patient with CCD, detailing genetic causes, clinical signs, and imaging results.
- The study aims to improve awareness and knowledge of CCD by reviewing existing literature on its manifestations and treatment options.
Article Abstract
Cleidocranial dysplasia (CCD) is a rare, congenital disorder characterized by a unique constellation of skeletal and dental abnormalities. The imaging findings, combined with clinical examination, help establish a definitive diagnosis. Understanding the broad spectrum of manifestations in CCD is essential for effective management and treatment. This case report aims to provide a comprehensive overview of a 25-year-old male patient with CCD, highlighting the genetic etiologies, clinical presentation, radiological findings, and a review of current literature to enhance understanding and awareness of this rare condition.
Download full-text PDF |
Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11319796 | PMC |
| http://dx.doi.org/10.7759/cureus.64456 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!