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1.
Strabismus ; 32(2): 108-114, 2024 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-38516834

RESUMEN

INTRODUCTION: To study the rare and unusual causes of monocular elevation deficit. METHODS: Five patients presenting to us with diplopia and elevation deficit were thoroughly examined and were found to have monocular elevation deficit due to rare causes. OBSERVATIONS: All five were found to have different underlying etiologies - iatrogenic, sphenoid wing meningioma, cysticercosis, sarcoidosis and mid brain infarct, and were managed appropriately. DISCUSSION: Monocular Elevation Deficit can occur due to a variety of causes. Having a high index of suspicion for the more serious etiologies is of utmost importance. Thorough clinical examination and imaging help clinch the diagnosis.


Asunto(s)
Diplopía , Meningioma , Humanos , Femenino , Meningioma/complicaciones , Masculino , Persona de Mediana Edad , Diplopía/etiología , Diplopía/fisiopatología , Diplopía/diagnóstico , Adulto , Neoplasias Meníngeas/complicaciones , Sarcoidosis/complicaciones , Sarcoidosis/diagnóstico , Sarcoidosis/fisiopatología , Cisticercosis/complicaciones , Cisticercosis/diagnóstico , Cisticercosis/fisiopatología , Enfermedad Iatrogénica , Infarto Encefálico/complicaciones , Infarto Encefálico/diagnóstico por imagen , Infarto Encefálico/fisiopatología , Anciano , Músculos Oculomotores/fisiopatología , Trastornos de la Motilidad Ocular/fisiopatología , Trastornos de la Motilidad Ocular/etiología , Trastornos de la Motilidad Ocular/diagnóstico , Imagen por Resonancia Magnética , Visión Monocular/fisiología , Hueso Esfenoides
3.
Indian J Ophthalmol ; 71(7): 2677-2686, 2023 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-37417105

RESUMEN

The optimal method of treatment for a child depends on the patient's age at the time of diagnosis, the onset and type of amblyopia, and the degree of compliance attainable. In deprivation amblyopia, the cause of visual impairment (e.g., cataract, ptosis) needs to be treated first, and then the disorder can be treated such as other types of amblyopia. Anisometropic amblyopia needs glasses first. In strabismic amblyopia, conventionally amblyopia should be treated first, and then strabismus corrected. Correction of strabismus will have little if any effect on the amblyopia, although the timing of surgery is controversial. Best outcomes are achieved if amblyopia is treated before the age of 7 years. The earlier the treatment, the more efficacious it is. In selected cases of bilateral amblyopia, the more defective eye must be given a competitive advantage over the comparatively good eye. Glasses alone can work when a refractive component is present, but occlusion might make the glasses work faster. The gold standard therapy for amblyopia remains occlusion of the better eye although penalization is also evidenced to achieve equal results. Pharmacotherapy has been shown to achieve suboptimal outcomes. Newer monocular and binocular therapies based on neural tasks and games are adjuncts to patching and can also be used in adults.


Asunto(s)
Ambliopía , Estrabismo , Niño , Adulto , Humanos , Ambliopía/terapia , Ambliopía/etiología , Agudeza Visual , Privación Sensorial , Estrabismo/terapia , Estrabismo/complicaciones , Refracción Ocular , Resultado del Tratamiento
4.
J AAPOS ; 27(2): 119-121, 2023 04.
Artículo en Inglés | MEDLINE | ID: mdl-36871930

RESUMEN

A 5-month-old girl presented with bilateral upper and lower eyelid cicatricial ectropion with right eye exposure keratopathy and bilateral lateral canthal defects. Physical examination revealed a constriction band over the temporal area of the head and nasal bridge; she was diagnosed with congenital amniotic band syndrome (ABS). Upper and lower eyelid reconstruction procedures were performed along with lateral canthal reconstruction to salvage the remaining left eye. Congenital ABS is a rare disorder. Most cases of ocular ABS are associated with limb deformities due to constriction defects and blood flow restrictions. Our patient presented solely with ocular and periocular deformities.


Asunto(s)
Síndrome de Bandas Amnióticas , Ectropión , Queratoconjuntivitis , Recién Nacido , Femenino , Humanos , Lactante , Síndrome de Bandas Amnióticas/complicaciones , Síndrome de Bandas Amnióticas/diagnóstico , Párpados/cirugía , Examen Físico
5.
Cornea ; 40(8): 1044-1047, 2021 08 01.
Artículo en Inglés | MEDLINE | ID: mdl-33935238

RESUMEN

PURPOSE: The purpose of this study was to report the analysis of reverse transcriptase polymerase chain reaction (RT-PCR) of nasopharyngeal (NP) samples of cornea donors dying because of causes unrelated to severe acute respiratory coronavirus (SARS-CoV-2). METHODS: A retrospective analysis of all cornea donors dying from causes other than SARS-CoV-2 between August 2020 and December 2020 was performed. Informed consent was obtained from the next of kin of the deceased for RT-PCR testing from NP swabs. Rapid antigen testing from all the deceased was performed before in situ cornea excision. In addition, NP samples in viral transport media for RT-PCR were also collected for SARS-CoV-2 analysis. Corneas were released from the eye bank only after a negative RT-PCR report. RESULT: One hundred eighteen corneas from 59 donors were obtained by the eye bank. Eleven donors (18.64%) were positive for SARS-CoV-2 on RT-PCR testing. Six of these 11 donors had a Ct value of E gene less than 25. CONCLUSIONS: NP samples of cornea donors dying due to causes other than coronavirus disease-19 were positive for SARS-CoV-2 on RT-PCR. This implicates that donors could be having asymptomatic/undetected coronavirus disease infection. We recommend adding the routine testing of NP samples of all cornea donors in the eye banking protocol in this ongoing SARS-CoV-2 pandemic.


Asunto(s)
Infecciones Asintomáticas/mortalidad , Prueba de Ácido Nucleico para COVID-19 , COVID-19/epidemiología , Bancos de Ojos/estadística & datos numéricos , Nasofaringe/virología , SARS-CoV-2/genética , Donantes de Tejidos/provisión & distribución , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Córnea , Humanos , Persona de Mediana Edad , ARN Viral/genética , Estudios Retrospectivos , Adulto Joven
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