{"id":11259,"date":"2025-07-27T03:56:16","date_gmt":"2025-07-27T01:56:16","guid":{"rendered":"https:\/\/valintermed.com\/?p=11259"},"modified":"2025-07-27T03:56:16","modified_gmt":"2025-07-27T01:56:16","slug":"sindrom-frinsa","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/frinsa-syndrome\/","title":{"rendered":"Fryns syndrome"},"content":{"rendered":"
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Fryns syndrome, also known as incomplete Edwards syndrome, is a rare genetic disorder caused by chromosomal abnormalities, primarily trisomy 18 or parts of it. The disorder is characterized by multiple abnormalities that can be detected by prenatal ultrasound or at birth. The most notable abnormalities include malformations of internal organs, dental abnormalities, nervous system disorders, and developmental disabilities. Although medical advances have improved the quality of life for these patients, treatment options remain limited, and more information about the disorder, its course, and treatment requires more detailed study and research.<\/p>\n

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