Abstract
Sickle cell disease (SCD) is an autosomal recessive hematological disorder that results in defective red blood cells (RBCs). These RBCs become sickled in shape, have a shortened lifespan leading to vascular occlusion and ischemia resulting in damaging effect on many organs throughout the body. There are numerous oral manifestations of SCD, although some may not be specific to SCD, it is important to recognize these clinical presentations and have a good understanding of the disease process to help in management of SCD from an oral health care perspective. The oral care of sickle cell patients requires specific precautions such as good management of local anaesthetics, rigorous anti-infective prophylaxis as well as controlled prescription of analgesics.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.