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1.
Perception ; 50(4): 367-378, 2021 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-33840289

RESUMEN

The objective of this study is to study the influence of ocular variables in the perception of #thedress and to develop a logistic regression model that could help predict it. This is a cross-sectional study on 1,100 subjects. People who did not report one of the two main perceptions were excluded from the study. Dress perception was codified as 0 (white&gold) or 1 (black&blue). The association between dress perception and demographic and main ocular variables (age, gender, binocular visual acuity, grade of nuclear cataract, crystalline lens status [phakic/pseudophakic], spherical equivalent, and ocular health status) was tested using logistic regression. Receiver operation curves were used to test the predictive value of the model. Several variables were found to be related with dress perception. The best model included three variables-Age: adjusted odds ratio (OR) = 1.02 (1.01-1.03), p = 0.08; ocular refraction: adjusted OR = 1.07 (1.02-1.12), p = 0.009; and nuclear cataract grade: adjusted OR = 1.45 (1.05-1.99), p = 0.026. The predictive value of the model was low (area under the curve = 0.62). Older age, nuclear cataract grade, and hyperopia were associated with black&blue perception. The predictive capacity of the developed model was poor. Only a small proportion of the variability in the #thedress perception can be explained by ocular examination.


Asunto(s)
Catarata , Percepción de Color , Anciano , Estudios Transversales , Ojo , Humanos , Refracción Ocular , Agudeza Visual
2.
PLoS One ; 11(1): e0146816, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-26784702

RESUMEN

The presence of more than one non-severe pathogenic mutation in the same mitochondrial DNA (mtDNA) molecule is very rare. Moreover, it is unclear whether their co-occurrence results in an additive impact on mitochondrial function relative to single mutation effects. Here we describe the first example of a mtDNA molecule harboring three Leber's hereditary optic neuropathy (LHON)-associated mutations (m.11778G>A, m.14484T>C, m.11253T>C) and the analysis of its genetic, biochemical and molecular characterization in transmitochondrial cells (cybrids). Extensive characterization of cybrid cell lines harboring either the 3 mutations or the single classic m.11778G>A and m.14484T>C mutations revealed no differences in mitochondrial function, demonstrating the absence of a synergistic effect in this model system. These molecular results are in agreement with the ophthalmological characteristics found in the triple mutant patient, which were similar to those carrying single mtDNA LHON mutations.


Asunto(s)
ADN Mitocondrial/genética , Mutación , Atrofia Óptica Hereditaria de Leber/genética , Adulto , Línea Celular , Respiración de la Célula , Femenino , Humanos , Mitocondrias/genética , Mitocondrias/metabolismo , Atrofia Óptica Hereditaria de Leber/metabolismo
3.
Int Ophthalmol ; 34(4): 1007-24, 2014 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-24604420

RESUMEN

Diplopia is a very disturbing condition that has been reported as a complication of several surgical procedures. The following review aims to identify the ocular and nonocular surgical techniques more often associated with this undesirable result. Diplopia is reported as an adverse outcome of some neurosurgical procedures, dental procedures, endoscopic paranasal sinus surgery, and several ophthalmic procedures. The most common patterns and some recommendations in order to prevent and treat this frustrating outcome are also given.


Asunto(s)
Diplopía/etiología , Procedimientos Quirúrgicos Operativos/efectos adversos , Humanos , Enfermedad Iatrogénica , Procedimientos Neuroquirúrgicos/efectos adversos , Procedimientos Quirúrgicos Oftalmológicos/efectos adversos , Procedimientos Quirúrgicos Orales/efectos adversos , Senos Paranasales/cirugía
4.
ISRN Ophthalmol ; 2011: 594848, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-24533187

RESUMEN

Infantile nystagmus is an involuntary, bilateral, conjugate, and rhythmic oscillation of the eyes which is present at birth or develops within the first 6 months of life. It may be pendular or jerk-like and, its intensity usually increases in lateral gaze, decreasing with convergence. Up to 64% of all patients with nystagmus also present strabismus, and even more patients have an abnormal head position. The abnormal head positions are more often horizontal, but they may also be vertical or take the form of a tilt, even though the nystagmus itself is horizontal. The aim of this article is to review available information about the origin and treatment of the abnormal head position associated to nystagmus, and to describe our treatment strategies.

5.
Arch Soc Esp Oftalmol ; 79(11): 549-52, 2004 Nov.
Artículo en Español | MEDLINE | ID: mdl-15578284

RESUMEN

CASE REPORT: An 18 year old female suffering from tuberculous meningitis with bilateral amaurosis, ophthalmoplegia, other cranial nerve palsies and loss of consciousness, is presented. DISCUSSION: Tuberculous meningitis is a rare cause of basal arachnoiditis with a bad prognosis. Possible causes of visual acuity loss and ophthalmoplegia are discussed and a favourable outcome without sequelae is noteworthy in our case.


Asunto(s)
Ceguera/etiología , Oftalmoplejía/etiología , Tuberculosis Meníngea/complicaciones , Adolescente , Femenino , Humanos
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