{"id":13219,"date":"2024-08-23T03:15:44","date_gmt":"2024-08-23T01:15:44","guid":{"rendered":"https:\/\/valintermed.com\/?p=13219"},"modified":"2024-08-23T03:15:44","modified_gmt":"2024-08-23T01:15:44","slug":"tetrasomiya-x","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/tetrasomiya-x\/","title":{"rendered":"Tetrasomy X"},"content":{"rendered":"
<\/div>\n

Tetrasomy X, also known as 49,XXXX syndrome, is a genetic disorder characterized by the presence of four extra X chromosomes in the body's cells, resulting in a complex pattern of phenotypic manifestations that affect both physical and psychosocial health. The condition occurs exclusively in females and is a form of chromosomal abnormality that belongs to a group of sex chromosome syndromes. The clinical manifestations of tetrasomy X can range from near normal to severe physical and cognitive impairment. Common symptoms include growth retardation, mental retardation, and a variety of structural abnormalities, including cardiovascular problems and skeletal abnormalities. The discovery and further study of this syndrome have contributed to a better understanding of chromosomal abnormalities and their impact on human health.<\/p>\n

\n
\n

Content<\/p>\nToggle<\/span><\/path><\/svg><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n