Results 1 to 10 of about 235 (61)
Displasias: Frontonasal y Frontofacionasal. Reporte de casos [PDF]
Salud Uninorte, 2015 Objetivo: Reportar dos casos clínicos encontrados en la consulta externa de Dismorfología de una institución de tercer nivel de atención de la ciudad de Cali, enmarcados dentro del espectro displasia frontonasal, anomalías congénitas raras, de las cuales
Jenny Ramírez-Gil +4 more
doaj +6 more sources
Brazilian Journal of Otorhinolaryngology, 2011 Frontonasal dysplasia (FND) is a rare malformative complex affecting the frontal portion of the face, the eyes and the nose; it may occur singly or associated with other clinical signs.
Melissa Zattoni Antoneli +4 more
doaj +2 more sources
Disostosis frontonasal acromélica (variante rara de displasia frontonasal)
Iatreia, 2010 Introducción: la Disostosis frontonasal acromélica (DFNA) es un subtipo poco frecuente de Displasia Frontonasal(DFN) de causa desconocida. Se sugiere herencia autosómica dominante. Los pacientes descritos presentan malformaciones frontonasales asociado a
Adriana Isabel Iglesias González +2 more
doaj +1 more source
Análise angular do corpo caloso em 18 pacientes com displasia frontonasal [PDF]
, 2015 Considering the rarity of the frontonasal dysplasia (FD) and the few reports about it in a large casuistry using magnetic resonance image (MRI), we describe the results of the angular analysis of the corpus callosum of 18 individuals with FD (7 male, 11 ...
Giffoni, Silvyo David Araújo +3 more
core +3 more sources
Encefalocele parieto occipital: Importancia de un diagnóstico precoz [PDF]
, 2023 The clinical manifestations of occipital encephalocele are usually rare, reaching a probability of 1 case per 10,000 pregnancies or 1 live birth with OE per 5,000 to 10,000 pregnancies and whose causes may be related to environmental, congenital factors.
Arley Yela, Hamilton +5 more
core +2 more sources
Arquivos de Neuro-Psiquiatria, 2007 In order to contribute to clinical delineation of midline facial defects with hypertelorism (MFDH) and to etiologic diagnosis of the isolated form, 31 patients with MFDH unaffected by known syndromic associations were evaluated. Group A included patients
Vera Lúcia Gil-da-Silva-Lopes +1 more
doaj +1 more source
Salud y enfermedad en el arte prehispánico de la cultura Tumaco : La Tolita II [PDF]
, 2018 Este libro presenta los resultados del proyecto de Investigación Salud y enfermedad en el arte prehispánico de la cultura Tumaco La Tolita II (300 a. C.-600 d.c) realizado entre 2007 y 2008 y que tenía como objetivo principal hacer un estudio sobre los ...
+3 more
core +4 more sources
Arquivos de Neuro-Psiquiatria, 2006 The aim of this study were to describe and to compare structural central nervous system (CNS) anomalies detected by magnetic resonance image (MRI) and computed tomography (CT) in individuals affected by midline facial defects with hypertelorism (MFDH ...
Vera Lúcia Gil-da-Silva-Lopes +1 more
doaj +1 more source
A ausência de mutações no gene PAX6 em três casos de síndrome de Morning Glory associada à deficiência isolada de hormônio do crescimento [PDF]
, 2008 Morning glory syndrome (MGS) is a congenital optic disc dysplasia often associated with craniofacial anomalies, especially basal encephalocele and hypopituitarism. Clinical signs are varied and often occult.
D'Souza-li, Lilia Freire Rodrigues +9 more
core +3 more sources
Hemangiomas faciales y diagnósticos diferenciales: reporte de tres casos colombianos con diagnóstico de asociación PHACE [PDF]
, 2015 Los hemangiomas son los tumores benignos más comunes en la infancia, su localización principal son cabeza y cuello. En esta región los hemangiomas suelen ser aislados, sin embargo cuando son segmentarios se asocian frecuentemente a anomalías sistémicas ...
Contreras García, Gustavo Adolfo +2 more
core +2 more sources