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1.
J Fr Ophtalmol ; 8(12): 785-8, 1985.
Artículo en Francés | MEDLINE | ID: mdl-3833889

RESUMEN

The authors have demonstrated a significant decrease of the plasmatic ionized calcium level in 84 patients during retinal fluorangiography likely due to a chemical bond between calcium and fluorescein. The side effects noticed during the procedure were similar to that quoted in the literature; their frequency, however, was not correlated with the decrease of the plasmatic ionized calcium level, even though the magnitude of the decrease was twice as great in the patients who experienced some trouble as in those who did not. This lack of correlation may be related to the too small patients sample. A greater frequency of side effects has been noticed in patients treated by calcium inhibitors.


Asunto(s)
Calcio/sangre , Angiografía con Fluoresceína , Fluoresceínas/efectos adversos , Bloqueadores de los Canales de Calcio/efectos adversos , Enfermedades Cardiovasculares/etiología , Femenino , Fluoresceína , Fluoresceínas/administración & dosificación , Fluoresceínas/metabolismo , Humanos , Concentración de Iones de Hidrógeno , Inyecciones Intravenosas , Masculino , Persona de Mediana Edad , Náusea/inducido químicamente , Náusea/etiología , Parestesia/inducido químicamente , Parestesia/etiología
2.
Acta Ophthalmol Scand ; 76(4): 509-12, 1998 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-9716345

RESUMEN

PURPOSE: Rieger Syndrome (RS) is an autosomal dominant disease, in which Axenfeld's and Rieger's anomalies are associated with typical facial dysmorphism and other extra-ocular findings. Cardiovascular defects are considered an occasional finding in this syndrome. METHODS: We describe a RS case in which the typical ocular and dysmorphic features were associated with bicuspid aortic valve. A review of the literature is provided. RESULTS: A total of 15 other cases of Axenfeld's or Rieger's anomaly associated with cardiovascular defects have been reported. In the cases in which the diagnosis of RS could be clinically performed, the cardiac defect mostly involved the outflow tract structures. CONCLUSION: The hypothesis that this association could be non-coincidental is discussed. The proved genetic heterogeneity of RS, based on clinical and molecular evidence, may suggest that RS is a contiguous gene syndrome or RS with cardiac defect is a separate entity. Finally we suggest a careful cardiological evaluation in RS patients, to assess the real frequency of cardiac defects in this syndrome.


Asunto(s)
Anomalías Múltiples/genética , Segmento Anterior del Ojo/anomalías , Estenosis de la Válvula Aórtica/congénito , Cara/anomalías , Iris/anomalías , Niño , Humanos , Masculino , Síndrome
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