Results 61 to 70 of about 584 (152)
Dental Press Journal of Orthodontics, 2010 O presente trabalho versa sobre o diagnóstico e a abordagem ortodôntica das anomalias dentárias, enfatizando os aspectos etiológicos que definem tais irregularidades de desenvolvimento. Parece existir uma inter-relação genética na determinação de algumas
Daniela Gamba Garib +3 more
doaj +1 more source
The FASEB Journal, Volume 40, Issue 12, 30 June 2026.Retinoic acid (RA) regulates the positional identity of cranial neural crest cells (CNCCs) through the transcription factors Alx1 and Alx4. Upon receiving RA from the local environment, liganded RAR/RXR heterodimers activate the expression of Alx1 and Alx4, which promote the frontonasal identity of CNCCs and inhibit the first pharyngeal arch identity ...
Shuxuan Wu +7 more
wiley +1 more source
Defeito de desenvolvimento de esmalte em dente permanente resultante de entubação orotraqueal nos primeiros anos de vida [PDF]
RGO: Revista Gaúcha de OdontologiaRESUMO Os defeitos de desenvolvimento de esmalte são alterações resultantes de distúrbios no processo da amelogênese, podendo envolver fatores genéticos, sistêmicos, locais ou ambientais.
Raphaela Magalhães Coimbra +4 more
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 6, June 2026.Clinical timeline of the reported EDSS1 case, illustrating disease onset, diagnostic milestones, treatment initiation, treatment modifications, and longitudinal response to combined topical minoxidil and tretinoin therapy from infancy through the last follow‐up.
Bana O. Aburajab +3 more
wiley +1 more source
Tamaño mesio-distal en pacientes con agenesia dental. Estudio de casos y controles
, 2020 Introducción. La agenesia dental es una de las anomalías de desarrollo bucal más frecuentes en el ser humano y se ha comprobado su relación con otras anomalías asociadas a la genética de este padecimiento.
ISIS GUADALUPE OLAIS ARJONA
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Análisis mutacional del gen MSX1 en pacientes con FLPNS e hipodoncia
Revista Universitas Medica, 2009 Introducción. La etiología de la hendidura labio-palatina es compleja e involucra factores genéticos y ambientales. Además de la hendidura, numerosos estudios han reportado la presencia de anomalías dentales en asociación con varias formas de hendidura ...
SANDRA JANETH GUTIÉRREZ PRIETO +3 more
doaj
Oral findings in patients with Apert Syndrome Achados bucais em pacientes com Síndrome de Apert
Journal of Applied Oral Science, 2006 INTRODUCTION: The Apert syndrome is a rare disorder of autosomal dominant inheritance caused by mutations in the FGFR2 gene at locus 10q26; patients with this syndrome present severe syndactyly, exophthalmia, ocular hypertelorism and hypoplastic midface ...
Gisele da Silva Dalben +2 more
doaj +1 more source
Homo luzonensis and the role of homoplasy in the morphology of hominin insular species
Cladistics, Volume 42, Issue 3, Page 286-316, June 2026.Abstract Homo luzonensis lived during the upper Pleistocene in the northern Philippines, east of the Wallace line. The few specimens attributed to this species show a mosaic of plesiomorphies for the genus Homo and apomorphies found in upper Pleistocene Homo species.
Pierre Gousset +4 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 5, May 2026.ABSTRACT Adhesive cantilever resin‐bonded bridges (RBBs) are a minimally invasive option for replacing maxillary lateral incisors in young cleft patients, in whom implant placement is often delayed until completion of craniofacial growth or declined due to surgical burden. Beyond material selection, the outcome depends critically on abutment design and
Aspasia Pachiou +3 more
wiley +1 more source
Agenesia dental en pacientes jóvenes.
, 2011 La agenesia dental o ausencia dental congénita, es un síndrome que se manifiesta en diversas poblaciones del mundo y genera múltiples consecuencias si su diagnóstico no se realiza oportunamente.
Rodríguez, Adriana M. +1 more
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