{"id":11934,"date":"2025-06-17T00:53:24","date_gmt":"2025-06-16T22:53:24","guid":{"rendered":"https:\/\/valintermed.com\/?p=11934"},"modified":"2025-06-17T00:53:24","modified_gmt":"2025-06-16T22:53:24","slug":"sindrom-mikroftalmii-lentsa","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/microphthalmia-lentsa-syndrome\/","title":{"rendered":"Lenz microphthalmia syndrome"},"content":{"rendered":"
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Lenz microphthalmia syndrome is a rare genetic disorder characterized by a complex of congenital anomalies in the development of the eyes and other organs. The key symptom of the pathology is microphthalmia, a decrease in the size of the eyeball, combined with other ophthalmological disorders such as coloboma of the iris, cataracts, and glaucoma. In addition to ocular manifestations, the syndrome is accompanied by multiple systemic anomalies affecting the skeletal system, kidneys, cardiovascular system, and other organs. According to research, the disease demonstrates pronounced clinical polymorphism even among members of the same family.<\/p>\n

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