{"id":11925,"date":"2025-06-17T03:01:14","date_gmt":"2025-06-17T01:01:14","guid":{"rendered":"https:\/\/valintermed.com\/?p=11925"},"modified":"2025-06-17T03:01:14","modified_gmt":"2025-06-17T01:01:14","slug":"sindrom-lou","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/low-syndrome\/","title":{"rendered":"Lowe's syndrome"},"content":{"rendered":"
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Lowe syndrome is a rare genetic disorder characterized by a triad of major symptoms: congenital cataracts, hypoplasia of the anterior chamber of the eye, and skeletal abnormalities. This X-linked recessive disorder predominantly affects males and causes severe visual impairment, multiple joint dysplasia, and characteristic physical dysmorphia. The pathogenesis of the disease is associated with impaired intracellular transport of proteins and lipids, which leads to complex disorders in various organs and systems of the body.<\/p>\n

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