Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 6 de 6
Filtrar
Más filtros

Tipo del documento
Intervalo de año de publicación
1.
Artículo en Inglés | LILACS, BBO | ID: biblio-1155002

RESUMEN

ABSTRACT Objctive: To assess the soft tissue characteristics of Bangladeshi adults to formulate soft tissue 3D CT standards using Holdaway's (HA) and lip morphology (LM) analyses. Another aim of this study was to assess the gender dimorphism of Bangladeshi population. Material and Methods: One hundred and seventeen (Eighty-five men and Thirty-two women) Bangladeshi adults have obtained their computed tomography (CT) scan at the Radiology Department for normal diagnosis. Craniofacial deformities were undetected in all cases. The CT images were prepared by a 3D imaging programming software (Mimics 11.02 Materialise). Parameters from the identified landmark points were measured in 3D through this software. Results: Upper lip thickness (ULT) (vermillion UL-A point) measurement was significant in HA and in LM analyses, upper lip protrusion (ULP) (Ls to Sn-SPog) measurement has demonstrated significant difference among both genders, where p-value was less than 0.05. Mean measurements of Bangladeshi adults were relatively comparable except the face convexity (FC) when compared with the HA cephalometric soft tissue values. Conclusion: By using HA and LM analyses, 3D CT soft tissue standards were established for Bangladeshi adults. Measurements for all parameters have remained equivalent with the HA standard data apart from the FC measurement. This consequently may demonstrate that the Bangladeshi population retains a convex shape with a slight protrusive lip or retruded chin.


Asunto(s)
Humanos , Masculino , Femenino , Adulto , Ortodoncia Correctiva , Cráneo/diagnóstico por imagen , Diagnóstico por Imagen/instrumentación , Anomalías Craneofaciales/diagnóstico por imagen , Cara/diagnóstico por imagen , Tratamiento de Tejidos Blandos , Bangladesh/epidemiología , Tomografía Computarizada por Rayos X/instrumentación , Estudios Transversales , Estudios Transversales/métodos , Estudios Retrospectivos , Interpretación Estadística de Datos , Caracteres Sexuales
2.
Alcohol ; 81: 31-38, 2019 12.
Artículo en Inglés | MEDLINE | ID: mdl-31082506

RESUMEN

Early detection of prenatal alcohol exposure is critical for designing and testing effectiveness of interventional therapeutics. Choline supplementation during and after prenatal alcohol exposure has shown promising benefits in improving outcomes in rodent models and clinical studies. A sheep model of first trimester-equivalent binge alcohol exposure was used in this study to model the dose of maternal choline supplementation used in an ongoing prospective clinical trial involving pregnancies at risk for FASD. Pregnant sheep were randomly assigned to six groups: Saline + Placebo control, Saline + Choline, binge Alcohol + Placebo (light binging), binge Alcohol + Choline, Heavy binge Alcohol + Placebo (heavy binging), and Heavy binge Alcohol + Choline. Ewes received intravenous alcohol or saline on three consecutive days per week from gestation day (GD) 4-41 to mimic a first trimester-equivalent weekend binge-drinking paradigm. Choline (10 mg/kg in the daily food ration) was administered from GD 4 until term. On GD 76, 11 fetal ultrasonographic measurements were collected transabdominally. Heavy binge alcohol exposure reduced fetal Frontothalamic Distance (FTD), Mean Orbital Diameter (MOD), and Mean Lens Diameter (MLD), and increased Interorbital Distance (IOD) and Thalamic Width (TW). Maternal choline supplementation mitigated most of these alcohol-induced effects. Maternal choline supplementation also improved overall fetal femur and humerus bone lengths, compared to their respective placebo groups. Taken together, these results indicate a potential dose-dependent effect that could impact the sensitivity of these ultrasonographic measures in predicting prenatal alcohol exposure. This is the first study in the sheep model to identify biomarkers of prenatal alcohol exposure in utero with ultrasound and co-administration of maternal choline supplementation.


Asunto(s)
Colina/farmacología , Anomalías Craneofaciales/prevención & control , Etanol/efectos adversos , Animales , Anomalías Craneofaciales/inducido químicamente , Anomalías Craneofaciales/diagnóstico por imagen , Anomalías Craneofaciales/embriología , Modelos Animales de Enfermedad , Femenino , Trastornos del Espectro Alcohólico Fetal/diagnóstico por imagen , Trastornos del Espectro Alcohólico Fetal/prevención & control , Embarazo , Ovinos , Ultrasonografía Prenatal
3.
JAMA Pediatr ; 171(8): 771-780, 2017 08 01.
Artículo en Inglés | MEDLINE | ID: mdl-28586842

RESUMEN

Importance: Children who receive a diagnosis of fetal alcohol spectrum disorder may have a characteristic facial appearance in addition to neurodevelopmental impairment. It is not well understood whether there is a gradient of facial characteristics of children who did not receive a diagnosis of fetal alcohol spectrum disorder but who were exposed to a range of common drinking patterns during pregnancy. Objective: To examine the association between dose, frequency, and timing of prenatal alcohol exposure and craniofacial phenotype in 12-month-old children. Design, Setting, and Participants: A prospective cohort study was performed from January 1, 2011, to December 30, 2014, among mothers recruited in the first trimester of pregnancy from low-risk, public maternity clinics in metropolitan Melbourne, Australia. A total of 415 white children were included in this analysis of 3-dimensional craniofacial images taken at 12 months of age. Analysis was performed with objective, holistic craniofacial phenotyping using dense surface models of the face and head. Partial least square regression models included covariates known to affect craniofacial shape. Exposures: Low, moderate to high, or binge-level alcohol exposure in the first trimester or throughout pregnancy. Main Outcomes and Measures: Anatomical differences in global and regional craniofacial shape between children of women who abstained from alcohol during pregnancy and children with varying levels of prenatal alcohol exposure. Results: Of the 415 children in the study (195 girls and 220 boys; mean [SD] age, 363.0 [8.3] days), a consistent association between craniofacial shape and prenatal alcohol exposure was observed at almost any level regardless of whether exposure occurred only in the first trimester or throughout pregnancy. Regions of difference were concentrated around the midface, nose, lips, and eyes. Directional visualization showed that these differences corresponded to general recession of the midface and superior displacement of the nose, especially the tip of the nose, indicating shortening of the nose and upturning of the nose tip. Differences were most pronounced between groups with no exposure and groups with low exposure in the first trimester (forehead), moderate to high exposure in the first trimester (eyes, midface, chin, and parietal region), and binge-level exposure in the first trimester (chin). Conclusions and Relevance: Prenatal alcohol exposure, even at low levels, can influence craniofacial development. Although the clinical significance of these findings is yet to be determined, they support the conclusion that for women who are or may become pregnant, avoiding alcohol is the safest option.


Asunto(s)
Consumo Excesivo de Bebidas Alcohólicas/patología , Anomalías Craneofaciales/inducido químicamente , Anomalías Craneofaciales/diagnóstico por imagen , Trastornos del Espectro Alcohólico Fetal/patología , Efectos Tardíos de la Exposición Prenatal/inducido químicamente , Australia , Estudios de Cohortes , Anomalías Craneofaciales/patología , Facies , Femenino , Humanos , Lactante , Masculino , Embarazo , Efectos Tardíos de la Exposición Prenatal/patología , Prevalencia , Estudios Prospectivos , Cráneo/anomalías , Tomografía Computarizada por Rayos X
4.
Orthod Craniofac Res ; 19(4): 222-233, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-27506322

RESUMEN

OBJECTIVES: There is controversy regarding the relationship between mandibular position and alterations of the cranial base that provoke a more anterior location of the glenoid fossa. Artificially deformed skulls display marked alterations of the cranial base. This study evaluates mandibular changes as function of the morphology of the cranial base in these skulls. MATERIAL AND METHODS: A geometric morphometric study was performed on lateral cephalometric X-rays of three groups of skulls: 32 with anteroposterior deformity, 17 with circumferential deformity and 39 with no apparent deformity. RESULTS: In artificially deformed skulls, the cranial base was deformed causing the mandibular condyle to be in a more anterior position. There was a complete remodelling of the mandible involving narrowing and elongation of the mandibular ramus, rotation of the corpus of the mandible and increased vertical height of the symphysis. Forward displacement did not occur. Integration between mandible and cranial base is not altered by deformation of the skull. CONCLUSIONS: Deformity of the cranial vault exerts an influence on the mandible, supporting the theory of modular units in complete integration. This also supports the theory that mandibular prognathism is a multifactorial result and not a direct effect of displacement of the cranial base.


Asunto(s)
Cefalometría/métodos , Anomalías Craneofaciales/diagnóstico por imagen , Procesamiento de Imagen Asistido por Computador/métodos , Mandíbula/patología , Base del Cráneo/patología , Cráneo/diagnóstico por imagen , Cráneo/patología , Arqueología , Anomalías Craneofaciales/etnología , Anomalías Craneofaciales/etiología , Historia Antigua , Humanos , Indígenas Sudamericanos/etnología , Masculino , Mandíbula/crecimiento & desarrollo , Cóndilo Mandibular/patología , Perú/etnología , Análisis de Componente Principal , Prognatismo/etiología , Radiografía/métodos , Cráneo/crecimiento & desarrollo , Base del Cráneo/crecimiento & desarrollo
5.
HNO ; 53(3): 223-9, 2005 Mar.
Artículo en Alemán | MEDLINE | ID: mdl-15703883

RESUMEN

A still-born male fetus from the 19th century, fixed in formalin and presenting as diprosopia triophthalmica, was analysed by helical computer tomography and virtually reconstructed without damage. This rare, incomplete, symmetrical duplication of the face on a single head with three eyes, two noses and two mouths develops in the first 3 weeks of gestation and is a subset of the category of conjoined twins with unknown underlying etiology. Spiral computer tomography of fixed tissue demonstrated in the more than 100 year old specimen that virtual reconstruction can be performed in nearly the same way as in patients (contrast medium application not possible). The radiological reconstruction of the Munich fetus, here confined to head and neck data, is the basis for comparison with a number of imaging procedures of the last 3000 years. Starting with some Neolithic Mesoamerican ceramics, the "Pretty Ladies of Tlatilco", diprosopia triophthalmica was also depicted on engravings of the 16th and 17th century A.D. by artists as well as by the anatomist Soemmering and his engraver Berndt in the 18th century. Our modern spiral computer tomography confirms the ability of our ancestors to depict diprosopia triophthalmica in paintings and sculptures with a high level of natural precision.


Asunto(s)
Anomalías Craneofaciales/diagnóstico por imagen , Anomalías Craneofaciales/historia , Ilustración Médica/historia , Medicina en las Artes , Escultura/historia , Gemelos Siameses , Europa (Continente) , Historia del Siglo XV , Historia del Siglo XVI , Historia del Siglo XVII , Historia del Siglo XVIII , Historia del Siglo XIX , Historia del Siglo XX , Historia Antigua , Historia Medieval , Humanos , Interpretación de Imagen Radiográfica Asistida por Computador , Tomografía Computarizada por Rayos X/historia
6.
J Neuropathol Exp Neurol ; 56(10): 1147-57, 1997 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-9329459

RESUMEN

Cerebro-oculo-facial-skeletal (COFS) syndrome is a rare autosomal recessive disorder with microcephaly, severe mental retardation, and death in childhood. The pathogenesis is unknown. Neuropathological features of 8 children with COFS syndrome are presented. Seven of the children, ranging in age from 36 weeks gestation to 5 years 8 months, are of North American aboriginal background from Manitoba, Canada. The eight child is a 3-year-old Caucasian male. In all children there was severe microencephaly and mild ventriculomegaly. Cerebral myelination appeared to be delayed in one infantile case. Swollen ubiquitinated granular cells appeared in the white matter shortly after birth. Older children displayed cortical neuron loss, patchy or diffuse absence of myelin and gliosis in the white matter, and pericapillary and parenchymal mineralization in the globus pallidus and to a lesser extent the putamen and cerebral cortex. The cerebellum of older children exhibited severe degenerative changes involving the internal granular layer and Purkinje cell layer. The neuropathological changes, previously not well documented, suggest that COFS syndrome is associated with a degenerative process that begins in utero and affects many brain cell types. Similarities to Cockayne syndrome are discussed.


Asunto(s)
Encéfalo/patología , Anomalías Craneofaciales/patología , Encéfalo/diagnóstico por imagen , Cerebelo/patología , Niño , Preescolar , Anomalías Craneofaciales/diagnóstico por imagen , Femenino , Lóbulo Frontal/patología , Humanos , Indígenas Norteamericanos , Lactante , Recién Nacido , Discapacidad Intelectual/patología , Masculino , Manitoba , Microcefalia/patología , Células de Purkinje/patología , Estudios Retrospectivos , Síndrome , Tomografía Computarizada por Rayos X , Población Blanca
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA