Angiomatosis Cerebroretinal

Angiomatosis cerebroretinalis (angiomatosis of the retina and blood vessels) is characterized by clinical manifestations that make it possible to identify it as a genetic cause of the development of changes in the extracellular matrix in the eyes. Manifestations of angiomatosis may include drusen, latticework, vascular seeds, arcuate veining, and iron deposition. In individuals with severe forms, angiomatoses affect the retina (iron deposition), cerebral arteries and veins, due to poor elasticity and increased lumen, which can result in rupture of cerebral arteries and blood

**Angiomatosis** Cereuroretinal is a rare disease, which is a benign tumor (angioma) localized in the thickness of the retina, as well as in the choroid, which usually manifests itself in childhood. The disease occurs as a result of impaired development and growth of blood vessels.

**Characteristic clinical signs** are: - different tumor sizes; - the presence of light and dark lesions that have different sizes and shapes; - protrusion of the vitreous body. Angiomatous Cerevnoretinal disease occurs predominantly in women, which is associated with hormonal levels that contribute to the occurrence of such diseases. ! The disease is chronic and progresses very slowly. Tumors have irregular, blurry outlines. They are distinguished by uneven edges, inside them there is a pigmented area, which has a connection with the subarachnoid space. **Patients complain of the appearance of fog before the eyes**, the presence of blind spots. ! In severe forms of Cerebro-Retinal angiomatosis, symptoms of increased blood pressure occur. The presence of tumors on the retina can lead to deterioration of vision, and sometimes to complete loss. ! As a rule, there is a hereditary predisposition and there is a possibility of developing angiomatoses of Cerebral retinitis. An accurate diagnosis can be established only after consulting an ophthalmologist and performing an ultrasound examination of the organs and tissues of the eye.