Results 141 to 150 of about 867,107 (207)
ABSTRACT Objectives To delineate the craniofacial morphometric characteristics of Thai children with syndromic (SC) and non‐syndromic craniosynostosis (NSC) and to assess dental maturation relative to Chronological Age (CA). Methods This comparative cross‐sectional study evaluated 19 patients (SC: n = 13; NSC: n = 6; mean age 9.32 ± 2.67 years ...
Nutthakarn Ratanasereeprasert +7 more
wiley +1 more source
Orthodontic Treatment of a Congenitally Missing Maxillary Lateral Incisor
Clinicians agree that, regardless of gender or race, tooth agenesis has become more prominent in recent societies. The congenital absence of one or more maxillary lateral incisors poses a challenge to effective treatment planning for the restorative ...
Okadakage, Sakiko +4 more
core +1 more source
ABSTRACT Objectives To characterize External Crown Resorption (ECR) in patients with Syndromic Amelogenesis Imperfecta (SAI) associated with junctional epidermolysis bullosa (JEB). Materials and Methods A multicentre retrospective study was conducted at two centers (Germany and Chile).
Susanne Krämer +10 more
wiley +1 more source
The role of Rho GTPases in facial morphogenesis
The role of small GTPases, RHOA, RAC1, and CDC42 and pathway mediators is reviewed in the context of embryonic facial development. Lip fusion requires cytoskeletal remodeling during morphogenesis of the facial processes and during lip fusion. Fnm, frontonasal mass; lnp, lateral nasal process; mnp, medial nasal process; mxp, maxillary process; np, nasal
Isra Ibrahim, Joy M. Richman
wiley +1 more source
Clinical analysis of supplemental maxillary lateral incisors: a retrospective cross-sectional study. [PDF]
Meng S +5 more
europepmc +1 more source
ABSTRACT Background and Aims This study aimed to examine, for the first time, two sets of goals: (1) simultaneous effects of five sets of asymmetries in five facial features (midline shift, midline cant, mouth corner, nose deviation, chin deviation) plus judges' expertise level and demographics on facial beauty, and (2) thresholds of different ...
Soroor Samie +4 more
wiley +1 more source
Whole exome sequencing and cluster analysis reveal that EPB41L4A mutation may trigger tooth agenesis. [PDF]
Li TQ +6 more
europepmc +1 more source
Abstract Objectives Hereditary polyposis syndromes in children are rare, heterogeneous disorders associated with significant morbidity and long‐term risk of malignancy. Current data on their presentation, management, and outcomes in pediatric populations remain limited.
Shlomi Cohen +9 more
wiley +1 more source
Prevalence and patterns of congenital tooth agenesis in children: a mixed-method study on parental awareness. [PDF]
Selen MB +4 more
europepmc +1 more source
Hypodontia of primary and permanent dentition - A case report
Hypodontia/Oligodontia of both the primary and permanent dentition is a rare finding. This paper reports a rare case of multiple missing primary and permanent teeth in a 7-year-old female child of Asian origin.Keywords: Congenitally missing teeth, tooth ...
Navin H K
core

