Results 51 to 60 of about 6,065 (217)

Oral and dental status in children with intestinal failure: A descriptive cross‐sectional study

Journal of Parenteral and Enteral Nutrition, EarlyView.
Abstract Background Children with intestinal failure often experience feeding difficulties and complex daily care needs, yet their oral and dental health remains underexplored. We aimed to describe oral and dental health characteristics in pediatric intestinal failure.
Anat Guz‐Mark, Dror S. Shouval, Raanan Shamir, Esti Davidovich   +3 more
wiley   +1 more source

DENTAL ENAMEL HYPOPLASIA: literature review

, 2022
Enamel hypoplasias are problems caused by both endogenous and exogenous factors during the process of tooth enamel development, the structures affected by these aggressive agents are the enamel secreting cells and ameloblasts. Hypoplasias can be clinically characterized from mild white spots noticeable only during close clinical examinations to ...
Paulo, Moises Lucio de, França , Mayra Maria Coury de   +1 more
openaire   +1 more source

The needle study: Machine learning as a new method for case‐finding in celiac disease

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives Despite a well‐defined diagnostic work‐up, uncertainties persist regarding celiac disease (CeD) detection strategies in the general population. Machine learning (ML) algorithms offer promise in aiding medical decision‐making on clinical data.
Chiara Maria Trovato, Monica Montuori, Maria Ludovica Costanzo, Giusy Russo, Cosimo Ruggiero, Danila Volpe, Francesca Ferretti, Antonella Diamanti, Carlo Ciliberto, Salvatore Oliva   +9 more
wiley   +1 more source

Prevalência de defeitos de desenvolvimento de esmalte na dentição decídua e fatores materno - infantis associados [PDF]

, 2004
Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde. Programa de Pós-Graduação em Saúde Pública.Os defeitos de desenvolvimento do esmalte dental (D.D.E.) são utilizados em antropologia para revelar informações ...
Lunardelli, Sandra Espíndola
core  

Genetic Landscape of Hearing Loss in Brazilian Patients Reveals Population‐Specific Variants and Clinical Correlations

Clinical Genetics, EarlyView.
The Burden: Hearing loss (HL) is the most prevalent sensory disorder globally, affecting 1.5 million individuals in Brazil. The Gap: While > 150 genes are linked to HL, the genetic architecture in underrepresented populations like Brazil is poorly defined. The Problem: This lack of data limits diagnostic yield and the application of precision medicine.
Stella Diogo‐Cavassana, Danillo Alencar‐Coutinho, Rafaella Abreu‐Oberhuber, Maria Eduarda Paramo‐Neto, Jeanne Oiticica, Ricardo Ferreira Bento, Ana Carla Batissoco, Karina Lezirovitz   +7 more
wiley   +1 more source

Enamel hypoplasia in a Mesolithic (5900±100 BC) individual from Woźna Wieś (Poland): a case study

Anthropological Review, 2018
Modern anthropological research includes very sophisticated diagnostic methods. They allow us to obtain information that has not been available so far.
Tomczyk Jacek, Ostrowska Agnieszka
doaj   +1 more source

ГИПОПЛАЗИЯ ЭМАЛИ У СОБАК И КОШЕК

Ветеринарная патология, 2012
Amelogenesis imperfecta (enamel hypoplasia, enamel dysplasia) - is a hypoplasia of the superficial layer of the tooth, caused by a violation of enamel formation of the matrix or mineralization, characterized by quantitative and qualitative inferiority of

doaj  

ORAL FINDINGS AND CLINICAL BEHAVIOR IN PATIENT HAVING AUTOIMMUNE POLYENDOCRINOPATHY CANDIDIASIS ECTODERMAL DYSTROPHY (APECED) [PDF]

Journal of IMAB
Introduction: APECED (Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy) is a rare autosomal recessive disease with significant impacts on oral health, including oral candidiasis and varying degrees of enamel hypoplasia.
Kremena Markova, Nikolay Simeonov
doaj   +1 more source

CHARGE Syndrome: A Narrative Review and Update on Diagnosis, Assessment and Management

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Background CHARGE syndrome (CS) is a rare multisystemic genetic condition caused by a pathogenic variant in the DNA‐binding protein‐7 CHD7 gene. The condition affects the development of neural crest cells, which give rise to craniofacial structures, cranial nerves, ears, eyes and the heart, resulting in diverse and complex clinical features ...
Eleni M. van Gelder, Suzanna E. L. Temple, Niall Jefferson, David Brown, Kasee Stratton‐Gadke, Madelene Rich, Steve Rose, Kim Blake   +7 more
wiley   +1 more source

Alterações do esmalte dentário em crianças nascidas prematuras e/ou baixo peso: revisão de literatura [PDF]

, 2011
TCC (graduação) - Universidade Federal de Santa Catarina, Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Curso de Odontologia.O objetivo deste estudo de revisão foi verificar a associação e a prevalência dos defeitos de ...
Franceschi, Laís Bison
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