Trismus pseudocamptodactyly syndrome is a very rare autosomal dominant inherited disorder characterized by the inability to completely open the mouth (trismus) and the presence of abnormally short tendon units causing the fingers to curve (camptodactyly). Early diagnosis and management of this condition is important to prevent facial deformities in the patient. Reporting such a case is important as case reports are one of the sources of data for calculating the prevalence of rare diseases. Here, we report a case of trismus pseudocamptodactyly syndrome in an eight-year-old boy with a brief review of the literature.

The otherwise considered being one of the smallest and weakest teeth in the arch, mandibular second premolars have been found to almost double its size in macrodontia. Such anomalies of morphological alterations have caused the teeth to be more weak and prone to diseases, as accredited to the increased surface area and particular morphology. Bilateral mandibular second premolar macrodontia is an extremely rare dental anomaly with only 5 cases reported to date, among which the first case was reported in 1967 by Primack. This article focuses on a rare case report of bilateral macrodontia of mandibular second premolar in an 18year old male.

Trigeminal neuralgia(TN) is