Background: Down syndrome (DS) is a genetic disorder in which there is an increased risk of developing clinical comorbidities that require regular attention: health problems, alterations in maxillomandibular development, chewing and swallowing problems, as well as dietary habits that may influence diet and nutritional status. This study will analyze the frequency of occurrence of these factors with increasing age in this population. Methods: A descriptive cross-sectional study was conducted with 18 participants aged 30–45 years. The condition of orofacial structures, chewing and swallowing function and oral and eating habits were assessed to observe the frequency of occurrence of these problems with increasing age. Results: A high frequency...
Aim of the study The aim of this study was to evaluate the incidence of dental issues for children w...
Aim It is well reported in the scientific literature that there is a high level of periodontal disea...
Down syndrome (DS) represents the most common congenital chromosomal anomaly of the human species, w...
Down syndrome (DS) is a genetic disorder in which there is an increased risk of developing clinical...
Background: Down syndrome (DS) is a genetic disorder in which there is an increased risk of developi...
Down syndrome (DS) is an autosomal disorder associated with mental and physical involvement. The typ...
Articlehttp://deepblue.lib.umich.edu/bitstream/2027.42/96981/1/UMURF-Issue05_2008-CMarkova.pd
Introduction: Down Syndrome (DS) is an autosomal chromosomal abnormality that results from trisomy o...
Background: An oral condition that has largely been ignored in the Down syndrome population is patho...
Down syndrome (DS) is the most common aneuploidy to affect humans and occurs in approximately 1 of 7...
International audienceThe effects of Down syndrome (DS) include orofacial dysmorphology with neuro-m...
Several features and comorbidities in Down syndrome have nutritional implications and consequences. ...
The aim of the present study was to assess the periodontal condition of individuals with Down syndro...
Introduction: Down syndrome (DS) is a common genetic disorder caused by the presence of an extra chr...
Aim: The purpose of this study was to assess the periodontal condition of people with Down syndrome ...
Aim of the study The aim of this study was to evaluate the incidence of dental issues for children w...
Aim It is well reported in the scientific literature that there is a high level of periodontal disea...
Down syndrome (DS) represents the most common congenital chromosomal anomaly of the human species, w...
Down syndrome (DS) is a genetic disorder in which there is an increased risk of developing clinical...
Background: Down syndrome (DS) is a genetic disorder in which there is an increased risk of developi...
Down syndrome (DS) is an autosomal disorder associated with mental and physical involvement. The typ...
Articlehttp://deepblue.lib.umich.edu/bitstream/2027.42/96981/1/UMURF-Issue05_2008-CMarkova.pd
Introduction: Down Syndrome (DS) is an autosomal chromosomal abnormality that results from trisomy o...
Background: An oral condition that has largely been ignored in the Down syndrome population is patho...
Down syndrome (DS) is the most common aneuploidy to affect humans and occurs in approximately 1 of 7...
International audienceThe effects of Down syndrome (DS) include orofacial dysmorphology with neuro-m...
Several features and comorbidities in Down syndrome have nutritional implications and consequences. ...
The aim of the present study was to assess the periodontal condition of individuals with Down syndro...
Introduction: Down syndrome (DS) is a common genetic disorder caused by the presence of an extra chr...
Aim: The purpose of this study was to assess the periodontal condition of people with Down syndrome ...
Aim of the study The aim of this study was to evaluate the incidence of dental issues for children w...
Aim It is well reported in the scientific literature that there is a high level of periodontal disea...
Down syndrome (DS) represents the most common congenital chromosomal anomaly of the human species, w...