| REVIEW ARTICLE |
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| Year : 2014 | Volume
: 4
| Issue : 6 | Page : 147-152 |
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Hemophilia A: Dental considerations and management
Shilpa Padar Shastry1, Rachna Kaul1, Kusai Baroudi2, Dilshad Umar3
1 Vydehi Institute of Dental Sciences and Research Center, Bangalore, Karnataka, Saudi Arabia
2 Department of Restorative Dental Sciences, Al-Farabi College of Dentistry, Riyadh, Saudi Arabia
3 Department of Orthodontics, Al-Farabi College of Dentistry, Riyadh, Saudi Arabia
Correspondence Address:
Dilshad Umar
Fathimas, Jain Compound, Attavar, Mangalore, Karnataka
Saudi Arabia
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/2231-0762.149022
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Aim: To review hemophilia A with emphasis on its oral manifestations, investigations, and dental management. Materials and Methods: Search was conducted using internet-based search engines, scholarly bibliographic databases, PubMed, and Medline with key words such as "Hemophilia A," "factor VIII," "bleeding and clotting disorders," and "dental management." Results: Hemophilia comprises a group of hereditary disorders caused due to the deficiency of one or more clotting factors leading to prolonged clotting time and excessive bleeding tendencies. It is broadly divided into hemophilia A, B, and C, which occur due to deficiency of factor VIII, IX, and XI, respectively. Hemophilia A is an X-linked recessive hereditary disorder and is the most common of the three, accounting for 80-85% of the cases. Conclusion: Understanding this complex entity is very important for a dentist to provide appropriate dental treatment and avoid undesirable consequences. |
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