Non-syndromic oligodontia Report of a clinical case with 14 missing teeth
نویسندگان
چکیده
منابع مشابه
Non Syndromic Oligodontia: Case Report
Oligodontia is a rare genetic disorder which represents the congenital absence of more than six teeth in primary, permanent or both dentitions. It is usually a part of a syndrome and seldom occurs as an isolated entity. Genes responsible for non syndromic oligodontia are found to be MSX1 and PAX9 genes. In this case report a 13 year old boy is presented who had absence of all four second perman...
متن کاملNon-syndromic oligodontia: a case report.
BACKGROUND oligodontia is a condition with developmental absence of six or more permanent teeth excluding the third molars. It is a rare finding which has not been frequently documented in Nigerian children. OBJECTIVE to report a case of non syndromic oligodontia. METHODS The details of the clinical presentation, course and outcome of a 9-year-old child with oligodontia were reviewed. The c...
متن کاملNon-syndromic oligodontia in permanent dentition: a case report.
Tooth agenesis is one of the most common congenital anomalies seen in humans. Although absence of one or more teeth is common but absence of multiple teeth is rare. Oligodontia is a rare developmental anomaly, involving agenesis of six or more permanent teeth, excluding the third molars. The reported prevalence of oligodontia in permanent dentition is 0.14%. Oligodontia can present as an isolat...
متن کاملCase Report: Congenitally Missing Teeth
Congenitally missing of maxillary lateral incisors is one of the most common patterns of hypodontia. This paper presents a nine year old boy with congenital missing of lateral incisors. Familial history showed that, his mother, aunts, uncle and grandmother have also congenital absence of lateral incisors.
متن کاملNon-syndromic oligodontia in permanent dentition of monozygotic twins: report of a rare case.
AIM To report a case of non-syndromic oligodontia involving 26 permanent teeth in monozygotic twin sisters and to discuss the possible genetic etiology, inheritance pattern and associated dental anomalies of this condition. BACKGROUND Hypodontia constitutes one of the most common developmental anomalies in humans and is defined as developmental absence of one or more teeth with reported preva...
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ژورنال
عنوان ژورنال: Bangladesh Journal of Medical Science
سال: 1970
ISSN: 2076-0299,2223-4721
DOI: 10.3329/bjms.v10i3.8365