نتایج جستجو برای: microdontia

تعداد نتایج: 162  

2011
Seema D Bargale Shital DP Kiran

Abnormalities in size of teeth and number of teeth are occasionally recorded in clinical cases. True generalized microdontia is rare case in which all the teeth are smaller than normal. Mesiodens is commonly located in maxilary central incisor region and uncommon in the mandible. In the present case a 12 year-old boy was healthy; normal in appearance and the medical history was noncontributory....

Journal: :Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2009
Bilal Ahmed Nazia Yazdanie

Hypodontia and associated conditions like Hereditary Ectodermal Dysplasia (HED) and microdontia markedly influence on physical, functional and psychosocial maturation of the affected individuals. Thorough evaluation, proper counseling and careful treatment planning employing a multidisciplinary approach are keys to a successful, long-term management. This case report describes the prosthodontic...

Journal: :Indian pediatrics 2014
Ankur Singh Mustafa Tekin Michelle Falcone Seema Kapoor

BACKGROUND Labyrinthine Aplasia, Microtia and Microdontia (LAMM) syndrome is characterized by the complete absence of inner ear structures (Michel aplasia), microtia and microdontia. Hypophosphatemic rickets results from defects in the renal tubular reabsorption of filtered phosphate. CASE CHARACTERISTICS 13-year-old Indian girl presented with deafness since infancy and progressive wrist wide...

2013
Anita Singhal Parul Singhal Ranjan Gupta Kush Dev Jarial

Spondyloepiphyseal dysplasia (SED) is a descriptive term used for group of inherited disorders of bone growth resulting in short stature, skeletal abnormalities, and problems with hearing and vision. SED have three major forms, SED congenital, pseudoachondroplastic SED, and SED tarda. SED tarda is milder than SED congenita. True generalized microdontia is a rare condition in which all the teeth...

2016
Marco Antonio García Castillo Silvia Tavira Fernández

In human dentition characteristics, complex processes intervene that have a close relationship with the growth and development of the whole craniofacial complex mainly in bones such as the maxilla and the mandible. Dental morphology is determined by environmental and genetic factors which are in a dynamic relationship that may cause single, partial or complete anomalies in dental development. D...

2017
Leonardo Fernandes da Cunha Ubiracy Gaião Rafael Coutinho Silva Carla Castiglia Gonzaga Gisele Maria Correr

The aim of this paper is to describe a restorative approach to the cosmetic remodeling of the teeth of a young adult patient with right maxillary lateral hypodontia and left lateral microdontia. A conservative restorative management was proposed to improve smile esthetics by combining direct composite resins and ceramics. Initially, periodontal therapy and dental bleaching were performed. Subse...

2012
Arife Kapdan Alper Kustarci Burak Buldur Dilara Arslan Alper Kapdan

OBJECTIVE The aim of this study was to determine the prevalence of double teeth, hypodontia, microdontia, and hyperdontia of primary teeth in Turkish children. METHODS The study group comprised 1149 children (554 girls, 595 boys). The children were examined in twelve local nurseries in Sivas, Turkiye. Clinical data were collected by four dentists according to Kreiborg criteria; which includes...

2016
Ewa Krasuska-Sławińska Agnieszka Brożyna Bożenna Dembowska-Bagińska Dorota Olczak-Kowalczyk

AIM OF THE STUDY Chemotherapeutic treatment in children and adolescents carries a risk of congenital tooth disorders and dentinoma. Study objective is to assess the correlation between tooth abnormalities, early complications of multidrug chemotherapy, and chemotherapeutics used in different antineoplastic therapies in children and adolescents. MATERIAL AND METHODS Enamel defects (development...

2014
Elise Schaefer Maryline Minoux Julia Lauer Valérie Pelletier Matthieu Schmittbuhl Marie - Cécile Manière François Clauss Françis Veillon Sophie Riehm Corinne Stoetzel Helene Dollfus

LAMM syndrome (OMIM #610706) is a rare autosomal recessive syndrome characterized by the association of Michel aplasia, microdontia and malformation of the external ear. Different mutations in FGF3 gene were reported in several families presenting with this syndrome. Clinical features and genetic results observed in a family with LAMM syndrome are reported. The diagnosis of isolated Michel apla...

2009
Nigel M. King S. Tongkoom H. M. Wong

Aim: To investigate the prevalence of eight morphological and numerical anomalies in the primary dentition of southern Chinese and to compare the prevalences with those from different ethnic groups. Materials and Methods: The material used in the study consisted of plaster casts and standardized panalipse radiographs collected from 936 randomly selected 5-year-old children (493 males and 443 fe...

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