Results 161 to 170 of about 1,241,893 (352)
Mapping Dental Care for Children and Adolescents With Rare Diseases: A Brazilian Multicentre Study
ABSTRACT Objectives To describe the landscape of dental care provided by specialised centres for children and adolescents with rare diseases (RDs) in the state of Minas Gerais, southeastern Brazil. Methods A retrospective cross‐sectional study was conducted involving individuals aged 0–18 years with a confirmed diagnosis of a RD who received care at ...
Heloisa Vieira Prado +21 more
wiley +1 more source
Background: It is axiomatic that Pediatric dental anomalies and enamel hypoplasia (E.H) are routinely encountered in primary dentition and early detection and prudent management of the condition facilitates normal occlusal development.
Suzan Sahana +5 more
doaj
Functional implications of minor mandibular asymmetry: clinical and digital research on a sample of healthy patients [PDF]
OBJECTIVE.The aim of the study is to evaluate the influence that the mandibular asymmetry could have towards the other components of the Stomathognatic system and to further related structures from a functional point of view. MATERIALS and METHODS.
Di Paolo, C. +4 more
core +1 more source
Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification. [PDF]
Since 2013, the International Union of Immunological Societies (IUIS) expert committee (EC) on Inborn Errors of Immunity (IEI) has published an updated phenotypic classification of IEI, which accompanies and complements their genotypic classification ...
Ailal, Fatima +18 more
core
We identified a recurrent heterozygous MAX c.179G>A:p.Arg60Gln variant in two unrelated females affected with the emerging phenotypes of MAX‐associated polydactyly‐macrocephaly syndrome. We propose that genitourinary abnormalities, including Mayer–Rokitanski–Kuster–Hauser syndrome in one individual, are an expansion of the known phenotypes associated ...
Iftekhar A. Showpnil +9 more
wiley +1 more source
New Dental Anomalies in the Greater Japanese Shrew Mole Urotrichus talpoides (Eulipotyphla: Talpidae) [PDF]
Shinya Okabe +2 more
openalex +1 more source
FAM20A variants cause AI1G, marked by enamel defects, gingival overgrowth and ectopic calcifications. RNA sequencing of patient‐derived gingival fibroblasts showed dysregulated genes in adhesion, proliferation and signalling pathways. Functional assays revealed increased cell proliferation, impaired ECM interactions and osteogenesis, suggesting FAM20A ...
Kanokwan Sriwattanapong +9 more
wiley +1 more source
Kdf1 Regulates Molar Cusp Morphogenesis via the PI3K/AKT/mTOR Signalling Axis
Epithelial Kdf1 knockout disrupts molar cusp morphogenesis by promoting inner enamel epithelium proliferation and invagination via PI3K/AKT/mTOR signalling. ABSTRACT Keratinocyte differentiation factor 1 (Kdf1) reportedly plays a significant role in enamel formation.
Jiayu Wang +9 more
wiley +1 more source
Smile Stories: Investigating Pediatric Dental Anomalies a Cross-Sectional Study
Objective: Determination of the frequency and distribution of dental anomalies across different age groups and gender within the pediatric population. Study Design: Cross-sectional observational study.
Mehwash Kashif , Irum Munir Raja , Uzma Zareef , Amna Rehman , Sana Adeeba Islam , Nabeel Khan
doaj +1 more source
H1N1 infection during pregnancy specifically targets the fetal liver and lungs, triggering immune responses, tissue fibrosis and ferroptosis in parenchymal cells, ultimately leading to adverse pregnancy outcomes, offering insights into managing maternal H1N1 infections and their impact on fetal health.
Yuxi Jiang +11 more
wiley +1 more source

