Eruption hematoma is a macular elevation in the soft tissue of alveolar mucosa seen nearly during the tooth eruption. Commonly, it does not have any clinical symptoms. In most cases, the black dome shape appearance of eruption hematoma worries parents about malignancy. Since the physicians are often the firsts who examine the affected child, this lett...

introduction: complicated crown- root fractures, extended caries and iatrogenic destruction often result in insufficient sound tooth structures and compromise the biologic width. two common options for re-establishing flap with osseous surgery. although some advantages are related to these two options, but coronal movement of gingival and alveolar bone in orthodontic extrusion, esthetic problem...

Human eruption is a unique developmental process in the organism. The aetiology or the mechanism behind eruption has never been fully understood and the scientific literature in the field is extremely sparse. Human and animal tissues provide different possibilities for eruption analyses, briefly discussed in the introduction. Human studies, mainly clinical and radiological, have focused on norm...

we describe, the first case of phenobarbital-induced dress syndrome presenting as a lichenoïd eruption. a 49-year-old man had received phenobarbital for a cerebral metastasis. twenty-five days later, he developed a purplish skin eruption, odynophagia, oral mucosal erosion and fever. physical examination revealed a cervical lymphadenopathy and facial edema associated to a diffuse violaceous macu...

Cleidocranial dysplasia is an autosomal dominant condition caused by mutation of RUNX2, characterized by generalized dysplasia of the bones and teeth. Affected individuals have short stature, atypical facial features, and skeletal anomalies affecting mainly the skull and clavicle. The dental manifestations are mainly delayed exfoliation of the primary teeth and delayed eruption of the permanent...

BACKGROUND Cleft lip and palate (CLP) is the most common orofacial congenital malformation in live births. CLP can occur individually or in combination with other congenital deformities. Affected patients experience a number of dental, aesthetic, speech, hearing, and psychological complications and have a higher incidence of severe dental conditions. The purpose of this study is to characterise...

The runt-related transcription factor 2 gene (RUNX2), which is also known as CBFA1, is a master regulatory gene in bone formation. Mutations in RUNX2 have been identified in cleidocranial dysplasia (CCD) patients. CCD is a rare autosomal dominant skeletal dysplasia that is characterized by delayed closure of cranial sutures, aplastic or hypoplastic clavicle formation, short stature, and dental ...