Results 71 to 80 of about 10,716 (226)

Exploring Enamel Hypoplasia and Metabolic Impacts on Dental Structures in Chronic Kidney Disease: A Systematic Review and Meta-Analysis

Pakistan Journal of Medicine and Dentistry
Background: The loss of mineral homeostasis in patients with chronic kidney disease causes significant dental problems, including enamel hypoplasia and increased tooth damage. The current clinical treatments show an insufficient ability to resolve these
Sadaf Ambreen, Amna Farrukh, Muhammad Mustafa, Ashar Hussain, Irum Naz , Fatima Ali   +5 more
doaj   +1 more source

Subadult Stress in the Medieval and Early Modern Populations of Continental Croatia [PDF]

, 2009
Svrha rada jest analiza učestalosti i distribucije dva pokazatelja subadultnog stresa (cribrae orbitaliae i hipoplazije zubne cakline), njihove međusobne korelacije i njihova odnosa s pokazateljem nespecifičnih zaraznih bolesti – periostitisom. U radu je
Maja Pasarić, Mario Novak, Mario Šlaus
core   +1 more source

Factors influencing oral colonization of mutans streptococci in young children [PDF]

, 2007
The document attached has been archived with permission from the Australian Dental Association. An external link to the publisher’s copy is included.This paper aims to critically review current knowledge about the key factors involved in oral ...
Law, V., Seow, W., Townsend, G.
core   +1 more source

[Dental enamel hypoplasia apropos of a case].

Fogorvosi szemle, 1996
The developmental anomalies of dental hard tissues are relatively common in children. These anomalies can involve separately the enamel and they are due to many factors acting during odontogenesis. The paper deals with the main ethological factors and describes a case of idiopathic hypercalcemia.
M, Alberth, Z, Dicsöffy, G, Keszthelyi
openaire   +1 more source

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 661-672, March 2026.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

Application of quantitative light-induced fluorescence to determine the depth of demineralization of dental fluorosis in enamel microabrasion: a case report

Restorative Dentistry & Endodontics, 2016
Enamel microabrasion has become accepted as a conservative, nonrestorative method of removing intrinsic and superficial dysmineralization defects from dental fluorosis, restoring esthetics with minimal loss of enamel.
Tae-Young Park, Han-Sol Choi, Hee-Won Ku, Hyun-Su Kim, Yoo-Jin Lee , Jeong-Bum Min   +5 more
doaj   +1 more source

The Relationships Between Fluoride Intake Levels and Fluorosis of Late‐Erupting Permanent Teeth [PDF]

, 2017
Objectives To examine the relationships between fluoride intake levels and fluorosis of late‐erupting permanent teeth. Methods The current study used information collected from 437 children in the longitudinal Iowa Fluoride Study.
Aasenden, Baelum, Beltran-Aguilar, Bhagavatula, Burt, Cruz-Orcutt, Dean, Dean, DenBesten, Haavikko, Hong, Hong, Ishii, Kroon, Kumar, Larsen, Larsen, Levy, Levy, Levy, Levy, Maguire, Manji, McClure, McClure, Nelson, Palenstein Helderman, Pendrys, Pendrys, Pendrys, Pendrys, Pendrys, Ramires, Russell, Rwenyonyi, Shillingburg, Singh, Slayton, Sudhir, Tai, Thylstrup, United States Department of Health and Human Services, Warren, Whitford   +43 more
core   +2 more sources

Pathogenesis and potential therapeutic targets of trichorhinophalangeal syndrome; lessons obtained from animal studies

Developmental Dynamics, Volume 255, Issue 3, Page 228-245, March 2026.
Abstract Trichorhinophalangeal syndrome (TRPS) is a rare genetic disease inherited in an autosomal dominant manner. It occurs in 1 in 100,000 people globally and is caused by several types of mutations of the TRPS1 gene. Since the first human patient was reported in 1966, typical and atypical pathologies, disease courses, and treatment case ...
Naoya Saeki, Rinna Kanai, Sayuri Tatsuta, Shinichi Kawaguchi, Masatsune Itoh, Shinsuke Ohba, Makoto Abe   +6 more
wiley   +1 more source

Er:YAG Laser Dental Treatment of Patients Affected by Epidermolysis Bullosa

Case Reports in Dentistry, 2014
Aim. The purpose of this study was to evaluate the efficacy of Er:YAG laser used for treating hard dental tissue in patients with epidermolysis bullosa (EB). Methods.
Angela Galeotti, Vincenzo D’Antò, Tina Gentile, Alexandros Galanakis, Simona Giancristoforo, Roberto Uomo, Umberto Romeo   +6 more
doaj   +1 more source

Developmental and Post-Eruptive Defects in Molar Enamel of Free-Ranging Eastern Grey Kangaroos (Macropus giganteus) Exposed to High Environmental Levels of Fluoride. [PDF]

PLoS ONE, 2016
Dental fluorosis has recently been diagnosed in wild marsupials inhabiting a high-fluoride area in Victoria, Australia. Information on the histopathology of fluorotic marsupial enamel has thus far not been available. This study analyzed the developmental
Uwe Kierdorf, Clare Death, Jasmin Hufschmid, Carsten Witzel, Horst Kierdorf   +4 more
doaj   +1 more source