incontinentia pigmenti is a rare inherited disorder involving abnormalities of the skin, hair, eyes, musculoskeletal system, central nervous system, and the teeth. dental abnormalities are the most common manifestations of this disorder. the purpose of this case report was to present the clinical and radiological findings of a seven-year-old girl as well as the results of her five-year follow u...

OBJECTIVES This objective of this study was to evaluate the role a heavy metal- lead acetate in eruption rate hypo functional incisors albino Wistar rats. METHODOLOGY An experimental done animal house Post Graduate Medical Institute, Lahore since March 2019 2020. 34 adult rats were randomly divided into two groups (n=17 for each group) i.e., control and group. Right mandibular selected study. S...

Menkes disease is a rare, autosomal recessive disorder characterized by neuronal degeneration, abnormal hair, malformed connective tissue, mental retardation, and a life span of three years. Previously reported dental findings include a high arched palate, delayed eruption of secondary dentition, and open bite. The case of twin seven-year-old males with Menkes disease is presented, along with p...

the permanent successor is present, eruption of a submerged tooth may be delayed or redirected from its normal path into a malaligned position. If the permanent successor is absent, loss of dental arch space is likely, and a midline discrepancy may occur because the mesiodistal width of the primary submerged tooth is greater than that of the contralateral premolar. Also, overeruption of the opp...

Allopurinol is one of the causative drugs that induce fixed drug eruption (FDE). The lymphocyte transformation test (LTT) is a safe and reliable diagnostic procedure for drug allergy, but is reported to be rarely positive in patients with FDE. In the current case, we performed an LTT and successfully confirmed allopurinol as the offending drug. This case report suggests that an LTT should be an...

Amelogenesis Imperfecta (AI) is a hereditary enamel defect which is characterized by developmental abnormalities in the quantity and/ or quality of enamel. This condition has been associated with dental anomalies, including taurodontism, congenitally missing teeth, delayed eruption, crown resorption, pulpal calcifications and odontogenic fibromas. This paper presents two cases of AI which were ...

Cleidocranial dysplasia is an autosomal dominant heritable skeletal disorder. The characteristic features of cleidocranial dysplasia (CCD) may include hypoplasia of the clavicle, delayed closure of frontanelles, late tooth eruption, and other skeletal disorders. This case report describes clinical and radiographic manifestations at the age of 11 and 29 of a CCD patient, investigates the mutatio...

A case of a compound odontoma which caused delayed eruption of right maxillary central incisor in a ten year old girl is presented with clinical and radiographic findings. The patient presented with complaint of a hard painless swelling in the right anterior region of the maxilla and absence of right maxillary central incisor. After clinical examination, periapical and occlusal radiographs of t...