Results 41 to 50 of about 2,773 (156)
HeliyonObjectives: To analyse the pathogenic genes in a patient with hypohidrotic ectodermal dysplasia (HED) and explore the relationship between pathogenic genes and the oligodontia phenotype.
Yi Wu +6 more
doaj +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 +2 more sources
Management of extraction sites: From biological principles to clinical practice
Periodontology 2000, EarlyView.Abstract Objectives To provide a concise overview of the biological events and dimensional changes following tooth extraction and to summarize current therapeutic strategies for extraction site management, including alveolar ridge preservation (ARP), alveolar ridge reconstruction (ARR), partial extraction therapies (PET), and tooth autotransplantation (
Emilio Couso‐Queiruga +1 more
wiley +1 more source
BMC Oral Health, 2023 Background Progressive familial intrahepatic cholestasis is a heterogeneous group of disorders, leading to intrahepatic cholestasis, with the possibility of chronic liver failure and biliary cirrhosis.
Mina Yazdizadeh +6 more
doaj +1 more source
The role of Rho GTPases in facial morphogenesis
Developmental Dynamics, Volume 255, Issue 10, Page 931-944, October 2026.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
Molecular Basis and Clinical Spectrum of WNT10A‐Related Oligodontia
Clinical Genetics, Volume 110, Issue 1, Page 3-14, July 2026.Cellular Mechanism behind WNT10A phenotypes. ABSTRACT WNT10A mutations, a major genetic determinant of dental agenesis and ectodermal dysplasia, exert profound effects on craniofacial development. Although classified as rare disorders, these mutations account for more than half of oligodontia cases, reflecting their critical role.
Perennes Elise +5 more
wiley +1 more source
European Oral Research, 2020 Purpose To evaluate the association between third molar (M3) agenesis and hypodontia and oligodontia in pediatric patients by using panoramic radiography.Materials and Methods Panoramic radiographs of 1,471 patients (899 females; 572 males) and 5,884 ...
Meltem Tekbaş Atay +2 more
doaj +1 more source
Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese population. [PDF]
PLoS ONE, 2013 BACKGROUND: Dental agenesis is the most common, often heritable, developmental anomaly in humans. Although WNT10A gene mutations are known to cause rare syndromes associated with tooth agenesis, including onycho-odontodermal dysplasia (OODD), Schöpf ...
Huiying He +6 more
doaj +1 more source
Non-Syndromic Oligodontia in permanent dentition: A case report [PDF]
, 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 +1 more source
A Combination of Variants in SEPTIN9 and MSX1 Genes Leads to the Formation of Orofacial Clefts
Genes to Cells, Volume 31, Issue 4, July 2026.Double‐depleted Xenopus embryos of xMSX1 and xSEPTIN9 exhibited orofacial clefts, and wild‐type but not variants in human MSX1 and human SEPTIN9 mRNAs could rescue the phenotype of morphants, indicating that variants in MSX1 and SEPTIN9, each individually tolerated, synergistically disrupt craniofacial morphogenesis to cause orofacial clefts.
Udval Uuganbayar +13 more
wiley +1 more source