Results 81 to 90 of about 6,085 (217)

Severe Enamel Defects in Wild Japanese Macaques

International Journal of Zoology
Plane-form enamel hypoplasia (PFEH) is a severe dental defect in which large areas of the crown are devoid of enamel. This condition is rare in humans and even rarer in wild primates.
Ian Towle, Carolina Loch, Marina Martínez de Pinillos, Mario Modesto-Mata, Leslea J. Hlusko   +4 more
doaj   +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

Heart Transplant for Noncompaction Cardiomyopathy in NONO‐Related Syndromic Intellectual Disability

Molecular Genetics &Genomic Medicine, Volume 14, Issue 7, July 2026.
Silent NONO variant c.348G>A caused exon 4 skipping, frameshift, and nonsense‐mediated decay in a boy with neurodevelopmental delay and severe left ventricular noncompaction requiring heart transplantation in early childhood. Stable graft function at 14 years highlights favorable long‐term cardiac outcome; literature review confirms a recognizable ...
Julia S. Singer, Dorota Garczarczyk‐Asim, Miriam Michel, Thomas Müller, Lukas Hackl, Andreas R. Janecke   +5 more
wiley   +1 more source

Indirect veneer treatment of anterior maxillary teeth with enamel hypoplasia [PDF]

, 2010
Background: Nowadays, aesthetic rehabilitation becomes a necessity. It is affected by patient’s background, especially career, social and economic status.
Devi Eka Juniarti
core   +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, Benkirane‐Jessel Nadia, Anton Nicolas, Vandamme Thierry, Clauss François, Conzatti Guillaume   +5 more
wiley   +1 more source

Morquio’s Syndrome: A Case Report of Two Siblings

Case Reports in Dentistry, 2017
Morquio syndrome or MPS IVA is a rare type of lysosomal storage disease associated with highly specific dental abnormalities. We present two siblings with enamel hypoplasia and skeletal abnormalities.
Sathish Muthukumar Ramalingam, Daya Srinivasan, Sandhya ArunKumar, Joe Louis ChiriyanKandath, Sriram Kaliamoorthy   +4 more
doaj   +1 more source

Gingival and Periodontal Diseases and Conditions in Children and Adolescents: Consensus Report

Journal of Clinical Periodontology, Volume 53, Issue 7, Page 1068-1099, July 2026.
ABSTRACT Background The objectives of this Focused Workshop were to update the epidemiology, aetiology, risk factors, diagnosis and management of gingival and periodontal diseases and conditions in children and adolescents, and to explore the applicability of the 2018 Classification in children and adolescents.
Iain Chapple, Sotiria Gizani, Mariano Sanz, Dominique Declerck, Phoebus Madianos, Valerie Clerehugh, Monique Danser, Esti Davidovich, Janet Davies, Nikos Donos, Elisabeth Dursun, Elena Figuero, Filippo Graziani, Mervi Gursoy, Soren Jepsen, Clara Joseph, Moritz Kebschull, Norbert Kraemer, Tina Lambrinaki, Rodrigo López, David J. Manton, Joerg Meyle, Ana Molina, Lior Shapira, Cheryl Somani, Georgios Tsilingaridis, Svante Twetman, Nicola West, Biniyam Wondimu, Ferranti Wong, David Herrera   +30 more
wiley   +1 more source

Etiology and Considerations of Developmental Enamel Defects in Children: A Narrative Review

Journal of Pediatrics Review, 2019
Context: Dental enamel is the hardest and highly mineralized structure in human body. However, Developmental Enamel Defects (DEDs) may occur due to an interplay between multiple factors ranging from genetic inadequacy to environmental insults.
Prasad Krishnaji Musale, Abhishek Shrikant Soni, Sneha Sunil Kothare   +2 more
doaj  

Dental enamel Hypoplasia. Investigations on the Bones Exhumed from the Medieval Necropole of Lozova (Republic of Moldova), XIVth–XVth Centuries [PDF]

Memoirs of the Scientific Sections of the Romanian Academy, 2014
Dental hypoplasia is a developmental anomaly based on perturbations of amelogenesis. Hypoplasia defects are part of the unspecific quantitative indicators for the state of health and / or nutritional state during the formation of the dental buds. It is a
Robert Daniel Simalcsik, Angela Simalcsik, Vasilica Monica Groza   +2 more
doaj  

Dental Professionals' Attitudes Toward Treating Patients With Sensory Impairments: A Cross‐Sectional Survey

Special Care in Dentistry, Volume 46, Issue 4, July/August 2026.
ABSTRACT Aims To analyze and compare the attitudes, perceived barriers, and professional confidence of dental students and practicing dentists toward treating patients with sensory impairments, and to examine associations with prior clinical experience and personal connection to disability.
Amir Laviv, Amichai Dvir, Itzhak Agayev, Michael V. Joachim   +3 more
wiley   +1 more source