Results 71 to 80 of about 2,549 (207)
International Journal of Paediatric Dentistry, Volume 36, Issue 1, Page 140-152, January 2026.ABSTRACT Background Regional odontodysplasia (RO) is a rare developmental dental anomaly with unknown prevalence. Current knowledge is largely limited to individual case reports. Aim This study aims to present epidemiological data, clinical features, and radiographic characteristics of pediatric and adolescent patients with RO in South Korea. Design In
So Dam Lee +5 more
wiley +1 more source
Česká Stomatologie a Praktické Zubní Lékařství, 2012 Background: Tooth agenesis means absence or incomplete development of tooth. It is a common human anomaly, which according to Online Mendelian Inheritance in Man database affects approximately 20% of the population.
L. Gábrlíková
doaj +1 more source
Zdravniški Vestnik, 2020 Background: Ectodermal dysplasia is a rare hereditary disease, characterized by defects in the development of two to five tissues derived from the embryonic ectoderm. As a part of the manifestation, oligodontia can occur.
Sonja Zarkovic Gjurin +3 more
doaj +1 more source
Combined Mutations of LTBP3 and COL5A1A in Geleophysic Dysplasia
Case Reports in Medicine, Volume 2026, Issue 1, 2026.Geleophysic dysplasias (GDs) are uncommon genetically predisposed abnormalities that interfere with skeletal growth and formation. Several GD subtypes have different clinical manifestations. The current report presents the case of a 7‐year‐old Syrian boy with a medical history of repeated bone fractures and noticeable facial characteristics.
Adel Alsharei +10 more
wiley +1 more source
Early treatment of nonsyndromic oligodontia: a clinical case report
Bioscience Journal, 2017 This report aims to describe the clinical case of a 10-year-old male patient (R.C.B.C.), presenting nonsyndromic oligodontia with maternal family trait and absence of 22 permanent teeth.
Carolina Ribeiro Starling +3 more
doaj +3 more sources
Cephalometric Measurements Of Non-Syndromic Oligodontia In Early Dental Age In A Japanese Population
Clinical, Cosmetic and Investigational Dentistry, 2019 Hisayo Mayama,1 Yukinori Kuwajima,2 John D Da Silva,3 Shahrzad Khorashadi,2 R Frederick Lambert,2,4 Yoshiki Ishida,2 Shigemi Ishikawa-Nagai,2 Hiroyuki Miura,5 Kazuro Satoh1 1Division of Orthodontics, Department of Developmental Oral Health Science ...
Mayama H +8 more
doaj
Case Reports in Dentistry, Volume 2026, Issue 1, 2026.Understanding the anatomical variations between primary and permanent dentitions and familiarity with the internal and external root morphology are essential for dental practitioners to distinguish root morphological anomalies. A search in dental literature reveals the occurrence of monoradicular molars in primary dentition; especially the ...
Basim Almulhim, Hannah Wesley
wiley +1 more source
Isolated oligodontia: Case report and two years follow up [PDF]
, 2014 Oligodontia is defined as the congenitally missing of six or more teeth, excluding the third molars. Oligodontia can occur isolated or as a part of a syndrome.
Korkut, Emre +3 more
core
Non-Syndromic Oligodontia in permanent dentition: A case report
, 2014 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.
Gambhir, RS +3 more
core +2 more sources
Mutations in COL1A1/A2 and CREB3L1 are associated with oligodontia in osteogenesis imperfecta
Orphanet Journal of Rare Diseases, 2020 Background Osteogenesis imperfecta (OI) is a heterogeneous connective tissue disorder characterized by an increased tendency for fractures throughout life. Autosomal dominant (AD) mutations in COL1A1 and COL1A2 are causative in approximately 85% of cases.
Kristofer Andersson +5 more
doaj +1 more source