Results 41 to 50 of about 15,266 (165)
International Journal of Paediatric Dentistry, Volume 36, Issue 5, Page 715-722, September 2026.ABSTRACT Background The prevalence of molar‐incisor hypomineralisation (MIH) has garnered increasing attention, with a likely association to hypomineralised second primary molars (HSPM). Aim To elucidate the prevalence of MIH and its association with HSPM.
Timo Saxer +3 more
wiley +1 more source
Amelogenesis imperfecta in a family
Revista Cubana de Estomatología, 2018 Introduction: amelogenesis imperfecta consists of a group of hereditary disorders that affect the development of the dental enamel in such a way that the clinical appearance of all or almost all primary and permanent teeth is compromised.
Paula Hurtado-Villa +3 more
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Rehabilitación bucal de la amelogénesis imperfecta en dentición primaria con silicona de adición transparente [PDF]
, 2021 La amelogénesis imperfecta comprende un grupo heterogéneo de defectos del esmalte de origen genético, con alteraciones en el proceso de formación del tejido adamantino.
Guerra Pacheco, Mirian Melisa
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Revista de la Asociación Odontológica Argentina, 2011 Resumen La amelogénesis imperfecta (AI) es una anomalía de origen genómico que altera en diferente grado la estructura del esmalte produciendo problemas de autoestima, deterioro de la salud bucal en general y la consecuente disminución de la calidad ...
María Tenenbaum Batkis +2 more
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Astrocytes in Genetic Epilepsies: Supporting Actor or Key Player?
Journal of Neuroscience Research, Volume 104, Issue 8, August 2026.Astrocytes contribute to the pathophysiology of acquired epilepsy. However, less is known about their contribution to genetic epilepsy syndromes which often exhibit frequent comorbidity with neurodevelopmental and psychiatric disorders. Epileptic seizures are also frequently present in neurodevelopmental disorders.
Jenny Lange +4 more
wiley +1 more source
Revista de la Asociación Odontológica Argentina, 2012 Resumen Objetivos: La Amelogénesis imperfecta es una anomalía poco frecuente, heterogénea y hereditaria. El tejido particularmente afectado es el esmalte, con diferentes grados y formas de alteración; afecta tanto la salud bucal en general como el ...
María Tenenbaun Batkis, Susana M. Falbo, Marcela Siri, Ariela Borjas +3 more
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Epidermolysis Bullosa Classification and Current Approach to Diagnosis
Pediatric Dermatology, Volume 43, Issue S2, Page 5-15, August 2026.ABSTRACT Epidermolysis bullosa (EB) is a heterogeneous group of rare genodermatoses marked by skin fragility and bullae formation induced by minor trauma. Pathologic variants in at least 21 genes are associated with EB, grouped into four major subtypes based predominantly on the plane of cleavage within the skin.
Hannah E. Mumber, Marissa J. Perman
wiley +1 more source
Amelogenesis Imperfect, Enamel Hypoplasia and Fluorosis Dental - Literature Review
Revista Brasileira Multidisciplinar - ReBraM /Brazilian Multidisciplinay Journal, 2015 The developmental disorders of enamel are abnormalities of structure which can affect both dentitions. These abnormalities include amelogenesis imperfecta, enamel hypoplasia and dental fluorosis.
Flávia Magnani Bevilacqua +2 more
doaj +1 more source
A propósito de un caso de amelogénesis imperfecta [PDF]
, 2018 En el siguiente trabajo se presenta un caso clínico de amelogénesis imperfecta, en una paciente femenina de 16 años de edad, donde haremos referencia al diagnóstico de estas lesiones y su posterior tratamiento, eligiendo en este caso como opción de ...
De Andrea, Antonela +6 more
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Amelogenesis imperfecta with gingival calcification: a rare presentation
Brazilian Journal of Oral Sciences, 2015 The purpose of this article is to highlight the rare presence of gingival calcification with Amelogenesis Imperfecta. A case is presented of a 12-year-old girl with a defect of enamel in deciduous as well as permanent dentition with moderate amount of ...
Sunitha Carnelio, Nirmala Rao
doaj +1 more source