Results 81 to 90 of about 9,346 (255)
Hypodontia is a type of dental anomaly that can affect dogs, characterized by the congenital absence of up to six deciduous or permanent teeth. According to reports in the literature, the absence of a dental element is an incidental finding and the absence of the first premolar teeth is observed more frequently.
Larissa Martins Cardoso +5 more
openaire +1 more source
ABSTRACT Keratosis–ichthyosis–deafness (KID) syndrome is a rare autosomal dominant ectodermal disease caused by mutations in the GJB2 gene, which encodes the gap junction protein Connexin 26 (Cx26) located on Chr. 13q12.11. This study presents the first mortality analysis associated with KID syndrome, focusing on a case report of a Latin American ...
Leslie Patrón‐Romero +17 more
wiley +1 more source
ABSTRACT Introduction As survival of paediatric cancer improves, more emphasis is placed on late adverse effects. However, the dental and periodontal adverse effects of cancer treatments in children remain an underinvestigated complication. This study aims to investigate the prevalence of late clinical dental adverse effects (cDAE) in survivors of ...
Koen B. Krommenhoek +10 more
wiley +1 more source
ABSTRACT Objective This study aimed to investigate how much the field of view (FOV) can be decreased while still depicting the necessary anatomical structures. A secondary aim was to assess how many incidental findings were missed with a reduced FOV. Material and Methods In this retrospective study, 170 CBCT volumes from children with a mean age of 9.4
Tobias Regnstrand +4 more
wiley +1 more source
Aarskog Syndrome: Deep Phenotyping and Genomic Landscape of a New Cohort Including Adult Patients
This study presents the deep phenotyping data of 14 new Aarskog‐Scott syndrome patients with molecular confirmation. ABSTRACT Aarskog‐Scott syndrome (AAS, MIM#305400) is an X‐linked disorder characterized by recognizable facial features, short stature, and genitourinary and skeletal malformations.
Gozde Tutku Turgut +7 more
wiley +1 more source
Wilms Tumor in Children With AMER1/WTX Germline Pathogenic Variants: A Multicenter Case Series
ABSTRACT Background 10–15% of children with Wilms tumor (WT) have predisposing genetic syndromes. Somatic mutations are frequently identified; however, germline pathogenic variants in AMER1 are much less prevalent and are associated with osteopathia striata with cranial sclerosis (OSCS).
Insiyah Campwala +9 more
wiley +1 more source
Hypodontia in the permanent dentition: a study of its prevalence in Malaysian children
An investigation of the prevalence and distribution of hypodontia was carried out in Malaysian children between the ages of five to fifteen years. Hypodontia occurred in 2.8 per cent of these children.
Nik-Hussein Nik Moriah
doaj +1 more source
Meðferð sjúklings með meðfædda tannvöntun [PDF]
Neðst á síðunni er hægt að nálgast greinina í heild sinni með því að smella á hlekkinn View/OpenInngangur Meðfædd tannvöntun færri en sex fullorðinstanna að undanskildum endajöxlum (hypodontia) er álitin vera til staðar hjá um það bil 7-8% fólks samkvæmt
Ellen Flosadóttir,
core
Dental anomalies : prevalence and associations between them in a large sample of non-orthodontic subjects, a cross-sectional study [PDF]
Background: To analyze the prevalence and associations between dental anomalies detectable on panoramic radiographs in a sample of non-orthodontic growing subjects.
Borzabadi-Farahani, Ali +5 more
core +3 more sources
Oral Health Status of Children With a History of Liver Transplantation
This study examines the oral health of children who have undergone liver transplantation, highlighting dental development delays despite similar caries rates compared to their healthy peers. Findings emphasize the need for integrated dental‐medical care, focusing on dental age assessment and early intervention to optimize oral health outcomes in this ...
Güler Burcu Senirkentli +2 more
wiley +1 more source

