Objective and methods: In order to investigate exodontia related complications with HIV-1 immunodeficiency, a retrospective observational analysis reviewed patients’ chart for age, co-morbidity and blood test results before and after…
Objectives: Mallampati classification is a standard preoperative airway examination assessing mouth opening and structures within the oral cavity. Hypothesis of this study was there is a positive correlation between mallampati…
Background: Paediatric facial injury can lead to significant morbidity. Sociodemographic determinants in Scotland have not previously been reported. Aim: To analyse the pattern, time trends, and key sociodemographic determinants in…
Introduction: General somatic growth slows down, 4.4 months gestation, yet growth/development/maturation of neural brain-CB/somatic immune system continues, full ontological pace. Methods: This paper explores ontological significance of brain/CB and immune…
Cherubism is a rare autosomal dominant disease of the maxilla and mandible. Approximately 200 cases have been reported by medical journals with the majority being males. The cause of the…
Introduction: The aetiology of parotid duct injuries is thought to be frequently caused by penetrating injuries in the parotid region, blunt trauma, complication of parotid duct cannulation for sialography and…
Introduction: Sickle cell disease (SCD) is an autosomal recessive disorder of haemoglobins with known orofacial complications, namely jaw pain and lip numbness. Updated knowledge of SCD among dentists may improve…
Introduction: Sickle cell disease (SCD) is an autosomal recessive haemoglobinopathy. Although orofacial complications among SCD patients have been reported, their prevalence remains undefined. We therefore investigate the prevalence of jaw…
The fetus presenting as a patient has now become a reality for the majority of clinicians. The evolution of imaging techniques has dramatically increased our knowledge of embryology and presented…
Nowadays nobody in Colombia would question the fact that German surgeon Waldemar Wilhelm is the Father of Oral and Maxillofacial Surgery in our country. Trained as an oral and maxillofacial…
Introduction: Traditionally the suture technique most used is with Silk 3.0 or 4.0, but it facilitates biofilm accumulation, because the Silk has polifilaments and it needs to be removed. Now…
Introduction: Nasopharyngeal tubes have been used to decompress extensive odontogenic cysts following marsupialisation. Some patients report experiencing mucosal soreness and occlusal interference. In order to construct a flexible and durable…
Rehabilitation is a complex process of restoration of a previous state following a major change. This could be congenital deformity, or a secondary result from head and neck cancer, which…
Purpose: Methicillin-resistant Staphylococcus aureus is an unusual finding in abscesses of deep fascial planes of the neck. This case report highlights MRSA found in the deep neck spaces in an…
Elongated styloid process is an infrequently seen condition which is rather hard to diagnose, causes sore throat, foreign body sensation at deglutition or earache by stimulating the pharynx and cervical…
There are a number of educational resources available to trainees in OMFS. To date there has been no comprehensive review of the educational resources available to trainees and their opinions…
With the 2012 Olympics getting closer to us, the drive to succeed and enhance oneself is becoming more and more important to both the athletes and the common public. The…
In the modern implantology, bone grafting has become a frequent procedure to reconstruct alveolar bone resorption and defects in edentulous areas. The aim of this prospective clinical study was to…
Introduction: The mandibular ameloblastoma is a benign odontogenic tumor that develops from the remaining components of the enamel organ. It is a slow growing, locally aggressive tumor capable of causing…
Introduction: Gardner Syndrome is a dominant autosomal phenotypical variant of Familial Adenomatous Polyposis (FAP), due to mutations in the APC gene in the 5q21–22 chromosome. Its main features are multiple…
