Results 61 to 70 of about 628 (133)
Pigmentary Mosaicism: An Overview
JEADV Clinical Practice, Volume 4, Issue 3, Page 681-689, August 2025.Pigmentary mosaicism is reflected by a patterned hypo‐, hyperpigmentation, or both combined in cutis tricolour. Pigmentary mosaicism can be associated with extracutaneous features (mainly neurological, musculoskeletal or ophthalmological). Three main mechanisms are involved in the development of pigmentary mosaicism: mosaicism for a chromosomal ...
C. Colmant +3 more
wiley +1 more source
Suspected Non-Syndromic Oligodontia – A Rare Case with 13 Agenesis
Acta Medica Philippina, 2019 Oligodontia is a condition in which the patient has more than six ageneses, excluding the third molars. Whereas the absence of one tooth is quite common, oligodontia is a rare congenital condition that can happen with or without the syndrome. The condition happens due to disturbances during odontogenesis process.
Dian Lupita Sari, - +4 more
openaire +2 more sources
Non-syndromic oligodontia in permanent dentition: a rare case report
Archives of Oral Research, 2013 Objective: Tooth agenesis is one of the most common congenital anomalies seen in humans. Although ab¬sence of one or more teeth is common, absence of multiple teeth is rare. Oligodontia is a rare developmental anomaly, involving agenesis of six or more permanent teeth, excluding the third molars.
Parampreet Pannu +3 more
openaire +1 more source
“Mini Molar Tooth” Sign in POLR3B‐Associated Cerebellar Ataxia with Hypomyelinating Leukodystrophy
Movement Disorders Clinical Practice, Volume 12, Issue 10, Page 1659-1661, October 2025.
Luca Marsili +5 more
wiley +1 more source
Non-syndromic Oligodontia in Permanent Dentition of Monozygotic Twins: Report of a Rare Case
The Journal of Contemporary Dental Practice, 2010 Abstract 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 ...
Gadda, Rohit B. +2 more
openaire +2 more sources
Non-syndromic oligodontia: A case report
International Journal of Medical and Dental Case Reports, 2020 Tejavathi Nagaraj +3 more
openaire +1 more source
An Orthodontic Study of Non-syndromic Oligodontia: An Examination of Occlusion and Occlusal Support
The Bulletin of Tokyo Dental CollegeThe aim of this study was to analyze orthodontic data to investigate occlusal conditions, the relationship between malocclusion and the number of congenitally missing teeth, and occlusal support of maxillomandibular teeth in patients with oligodontia.
Tazuhama, Yasuko +5 more
openaire +2 more sources
Letter to Editor- Oligodontia in Non-syndromic Children: Series of Three Cases [PDF]
Journal of Clinical and Diagnostic Research, 2019 Fernanda Felix Da Silva +4 more
doaj +1 more source
Oral rehabilitation of non-syndromic oligodontia: A case report
International Journal of Applied Dental Sciences, 2022 Manoranjan Mahakur +6 more
openaire +1 more source
A Novel PAX9 Mutation in a Family with Non-Syndromic Oligodontia [PDF]
THE JOURNAL OF THE KOREAN ACADEMY OF PEDTATRIC DENTISTRY, 2016 Ye ji Lee +5 more
openaire +1 more source