Results 81 to 90 of about 5,474 (244)
Presentation of Bilateral Facial Paralysis in Melkersson–Rosenthal Syndrome
Introduction. Melkersson–Rosenthal syndrome (MRS) is a neuromucocutaneous disorder characterized by the following classic symptom triad: peripheral facial paralysis, orofacial edema, and scrotal or fissured tongue.
Gustavo Gaitan-Quintero +3 more
doaj +1 more source
Early Clinical Experiences for Dental Students Using Near Peer Assisted Learning (NPAL)
ABSTRACT Introduction This paper describes Doctor of Dental Surgery students' perspectives on participating in NPAL sessions at the School of Dentistry at the University of Alberta. NPAL provides early clinical experiences (ECE) for junior students (mentees) assisted by senior students (mentors).
Anthea Senior +4 more
wiley +1 more source
Tongue Lesions in Pakistani population, Subjective Awareness and Association with Blood Groups
Objective: To determine the frequency of various tongue lesions diagnosed during dental examination in a Pakistani population and to assess their association with blood groups. Study Design: Cross-sectional study.
Ambreen Gul +5 more
doaj +1 more source
Summary A 17‐year‐old Swiss Warmblood mare presented with signs of left‐sided facial nerve paralysis and was diagnosed with left‐sided temporohyoid osteoarthropathy (THO). A partial ceratohyoidectomy was performed in the standing, sedated mare to treat this condition.
J. Kuhlmann +5 more
wiley +1 more source
Consideraciones en el diagnóstico de psoriasis oral: presentación de un caso clínico [PDF]
Este artículo comenta las dificultades de hacer un diagnóstico definitivo de psoriasis oral basado en la evidencia clínica e histológica. Se presenta un joven varón negro con múltiples lesiones que muestran erosiones, fisuras y escaras amarillentas en el
Marques, M.M. +3 more
core +1 more source
Waardenburg syndrome type I: dental phenotypes and genetic analysis of an extended family [PDF]
Background: The aim of this study was to describe the pattern of inheritance and the clinical features in a large family with Waardenburg syndrome type I (WS1), detailing the dental abnormalities and screening for PAX3 mutations ...
Aquino, Sibele Nascimento de +8 more
core +1 more source
Pachyonychia congenita is an uncommon autosomal dominant skin disorder characterized by hypertrophic nail dystrophy, palmoplantar keratoderma, oral leukokeratosis, and cutaneous cysts.
Jiali Liang +7 more
doaj +1 more source
Transillumination‐Aided Infiltration of MIH‐Affected Molars: Evaluation of the Clinical Workflow
ABSTRACT Background Enamel affected by molar incisor hypomineralisation (MIH) exhibits reduced mechanical properties due to its disorganised prismatic structure, lower mineral density and higher protein content. These alterations increase porosity and susceptibility to posteruptive enamel breakdown.
Omar Marouane +5 more
wiley +1 more source
Periodontitis and Periodontal Conditions in Systemically Healthy Children and Adolescents
ABSTRACT Objective To answer the PICoS question ‘in systemically healthy children and adolescents (Population), what are the main features of periodontitis, necrotising periodontal diseases (NPD) and other periodontal conditions (periodontal abscesses, endo‐periodontal lesions, traumatic occlusal forces, prosthesis‐ and tooth‐related factors ...
Inbar Eshkol‐Yogev +5 more
wiley +1 more source
Prevalence of Tongue Anomalies in Hamadan, Iran [PDF]
Background: Since the earliest days of medicine, the tongue has been considered a good reflection of systemic disease. Hippocrates, Galen and others considered the tongue to be barometer of health.
F Mojarrad, P Bakianian Vaziri
doaj +2 more sources

