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Very often, anisometropia is diagnosed at an early age and is congenital. This may be accompanied by asymmetry in the face and skull. Sometimes the disease manifests itself in adolescents in the process of growing up, when the body begins to grow. This may be due to the uneven development of diflucan in both eyes. In other words, anisometropia happens: Hereditary. If someone in the family has already suffered from a similar pathology, there is a risk that the child will also be diagnosed with it. Acquired. It manifests itself after a previous eye disease, surgery or injury to the eyeball.
Causes of the onset of the disease in children: Congenital unilateral myopia. This is congenital myopia in a child, which can be leveled in the process of fluconazole pills. Heredity. If someone from the older generation had a similar pathology, in infants it can be inherited at birth.
In the process of developing anisometropia, the patient's central nervous system is protected from discomfort, since the visual analyzer is not able to add images of both eyes that are different in terms of indicators into one picture. For this reason, the image begins to be ignored, and the refractive error is further exacerbated. The consequence may be the extinction of the visual functions of one eye, which is often the cause of amblyopia.
Another complication of this pathology may be the development of strabismus (divergent or convergent). If treatment measures are started in a timely manner, the disease may not progress. Timely diagnosis will help prevent complications, followed by symptomatic or surgical correction.