Results 91 to 100 of about 5,325 (223)
Intestinal Involvement in Kawasaki Disease [PDF]
To describe a case of Kawasaki disease with intestinal involvement and to analyze other published reports to define clinical characteristics, diagnostic issues, and therapeutic approaches of gastrointestinal involvement in Kawasaki ...
Cascio, Antonio +9 more
core +1 more source
Epidemiología de la patología de la mucosa oral más frecuente en niños [PDF]
El odontólogo responsable de tratar al niño debe tener en cuenta la posibilidad de encontrar cualquier condición patológica a nivel de la mucosa oral sobre todo a edades tempranas.
Planells del Pozo, Paloma +2 more
core +1 more source
The oral microbiota and periodontal health in orthodontic patients
Abstract The oral microbiota develops within the first 2 years of childhood and becomes distinct from the parents by 4 years‐of‐age. The oral microbiota plays an important role in the overall health/symbiosis of the individual. Deviations from the state of symbiosis leads to dysbiosis and an increased risk of pathogenicity.
Brandon W. Peterson +4 more
wiley +1 more source
Differences in the morphological structure of the human tongue
BACKGROUND: The tongue exhibits significant individual variability in terms of shape, colour, and surface texture. Due to its location, it is easily accessible for medical examination, although often overlooked.
Klaudia Kulig +3 more
doaj +1 more source
Abstract For decades, osseous resective surgery along with apically positioned flap procedure has been advocated as a predictable treatment option to reduce residual pockets and minimize periodontal complications during supportive periodontal care. More recently, Fiber Retention Osseous Resective Surgery (FibReORS) has been suggested to reduce the ...
Gianfranco Carnevale +3 more
wiley +1 more source
Concurrent Occurrence of Ear Tag With Posterior Talon Cusp, Fissured Tongue, and Ankyloglossia: A Case Report. [PDF]
Sundaresan M +4 more
europepmc +1 more source
ABCA12 Frameshift Deletion in Domestic Cats With Ichthyosis Fetalis
ABSTRACT Background Ichthyosis fetalis (IF), also known as harlequin ichthyosis, is a rare and often fatal autosomal recessive congenital skin disorder. It is characterized by thickened, hard skin plaques and deep skin fissures that limit mobility and cause malformations of the eyes, lips and ears.
Jeanna M. Blake +2 more
wiley +1 more source
Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat +4 more
wiley +1 more source
Oral mucosa alterations in a socioeconomically deprived region: prevalence and associated factors
This study aimed to evaluate the prevalence and factors associated with oral mucosa alterations in patients from Vale do Jequiti-nhonha, Brazil. The sample consisted of 511 patients of both genders.
Raquel Gonçalves Vieira-Andrade +5 more
doaj +1 more source
ABSTRACT Objectives Dental caries is a global health concern caused by the formation of cariogenic biofilms and their acid production. While various approaches have been tried, the rise of antibiotic‐resistant microorganisms necessitates safer and more effective antimicrobial solutions.
Parisa Habibi +3 more
wiley +1 more source

