We are reporting here, a case of the Lenz syndrome in a neonate who was brought to the Paediatric OPD, Kasturba Medical College Hospital, Attavar, Mangalore India, with the complaints of poor suckling since birth and abnormal facial features. Altogether, the characteristic congenital abnormal findings in Lenz syndrome, which comprise of microophthalmia, ear anomalies, microcephaly, skeletal and...

The acronym CHARGE refers to a non-random clustering of congenital malformations whose cause remains unknown. To date, the dental features of CHARGE association are not well known. A brief review of the literature and a case in a 10-year old boy with the CHARGE association are presented. The patient had multiple dental anomalies including congenital absence of teeth, ectopic eruption, submergen...

Tel: +98 21 84902473 Fax: +98 21 84902473 Email: [email protected] Klinefelter syndrome includes a group of chromosomal disorders with at least one additional X chromosome in male karyotype (46,XY). Up to now, different dental manifestations such as taurodontism, congenital absence of permanent teeth, shovel incisors, occlusal anomalies and increased permanent tooth size have been reported...

The case of a 3 11/12-year-old Chinese boy with the dental abnormalities of "otodental" dysplasia is reported. Hearing was normal. Dental anomalies consisted of delayed eruption of globe-shaped molars, bulbous deciduous canines, and double pulp chambers in the molars. Radiographs taken 4 years later showed taurodontic molars, supernumerary microdontic teeth, retarded formation of premolars, and...

The symptom failure to thrive (FTT) is increasing in the general population, and has a prevalence of 9.6% among infants in the United States. Other factors occur in association with growth failure such as medical and dental anomalies and developmental delays that influence the management of these children. Four cases are presented to demonstrate the spectrum of problems and interdisciplinary ma...

Anomalies in amelogenesis may be due to developmental defects or abnormalities in different components of developing teeth and can affect dental development. We compared dental development in a group of children with molar-incisor hypomineralization (MIH) with that in age- and sex-matched controls. Dental age was determined using panoramic radiographs of 105 children (59 girls, 46 boys) aged 7-...

The diagnosis of many dental anomalies would be impossible without radiographs, because of their location in the mineralized tissues (bone and teeth) or because they are hidden under the surface of the cortical plate that cannot be seen during a visual examination in dental practices. The use of radiographs is indispensable during the treatment phase, e.g., during root canal treatment to monito...

The research objectives were to determine the prevalence of impacted teeth in orthodontic patients Israel, examining epidemiological and genetic linkage. Methods: Data was collected from cohort treated Tel-Aviv University between 2010–2017. Forty-five for randomly selected, compared 45 control patients, paired by age sex. Collected data included: week birth, type medical history, dental anomali...

Purpose. Craniofacial morphology is usualy described by the head (cephalic index) and face form (prosopic index). The aim of this study was to establish the existence of correlations between the cranial and facial types and the dento-maxillary anomalies. Material and Methods. Data were collected from two groups of patients (a control group of 42 patients without dental anomalies and a test grou...

INTRODUCTION Hereditary nonpolyposis colorectal cancer is a colorectal cancer syndrome characterized by the development of colorectal cancer and extracolonic tumors, and this syndrome has an autosomal dominant mode of inheritance. To our knowledge, our study was the first to find dento-osseous anomalies and the second to observe Fordyce granules in a family with individuals with hereditary nonp...