{"id":12960,"date":"2024-08-23T07:35:27","date_gmt":"2024-08-23T05:35:27","guid":{"rendered":"https:\/\/valintermed.com\/?p=12960"},"modified":"2024-08-23T07:35:27","modified_gmt":"2024-08-23T05:35:27","slug":"sindrom-svayera","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/sway-syndrome\/","title":{"rendered":"Swyer syndrome"},"content":{"rendered":"
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Swyer syndrome (or monochromosomal syndrome) is a rare genetic disorder caused by a disorder in the formation of sex chromosomes, specifically the absence of one of the Y chromosomes in males. This condition, which is a chromosomal abnormality, is characterized by the presence of 46 chromosomes (this is the normal chromosome set). Usually, males have a 46 XY chromosome set, but in Swyer syndrome, 45 X are found, which causes non-developing or underdeveloped genitals and other abnormalities. Patients have abnormalities of the gonads, which leads to insufficient levels of androgens and estrogens, which do not stimulate normal development of the reproductive system. In most cases, the syndrome remains undiagnosed until puberty, which makes its diagnosis and treatment especially important for ensuring the normal physical and psychological development of the individual.<\/p>\n

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