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Pathological conditions of craniosynostosis in aboriginal populations from the Gran Chaco plains of northwestern Argentina: A case report
(Wiley, 2019)
Theaim of this paper is to present a case report of craniosynostosis found in apre-Columbian population from Argentina. Craniosynostosis refers to theprematural closure of the cranial sutures and is primarily caused by ...
Apert syndrome: a case report in pediatric dentistrySíndrome de Apert. Reporte de caso en odontopediatría
(Universidad Nacional Mayor de San Marcos, Facultad de Odontología, 2011)
Low size for selective and idiopathic growth hormone deficiency associated with Crouzon SyndromeBaja talla por déficit selectivo e idiopático de hormona de crecimiento asociado al Síndrome de Crouzon
(Intituto Tecnológico de Santo Domingo (INTEC), 2017)
Array comparative genomic hybridization in confirmation of the deleted genes in a patient with subterminal deletion of the long arm of chromosome 10 associated with sagittal craniosynostosis and dysmorphic features
(BioMed Central, 2014)
Craniosynostosis results from premature ossification of
one or more cranial sutures and leads to alterations in
the shape of the skull and/or premature closure of cranial
fontanels, causing impairment of brain ...
Crouzon Syndrome, report of a fetal autopsySíndrome de Crouzon, reporte de una autopsia fetal
(Universidad Centroccidental Lisandro Alvarado, 2019)
Maxillary osteogenic distraction and comprehensive orthodontic treatment in a patient with Pfeiffer syndrome. A case reportDistracción osteogénica del maxilar y manejo ortodóncico integral en paciente con síndrome de Pfeiffer. Reporte de caso
(Universidad Nacional Mayor de San Marcos, Facultad de Odontología, 2019)
Case Report Familiar Benign Acanthosis Nigricans and Review of the Literature: Scientific Journal of Health and Human DevelopmentAcantosis Negricans Benigna Familiar. Reporte de Caso y Revisión de la Literatura
(Centro Latinoamericano de Investigación y Ciencias, 2024)