{"id":12951,"date":"2024-08-23T07:44:52","date_gmt":"2024-08-23T05:44:52","guid":{"rendered":"https:\/\/valintermed.com\/?p=12951"},"modified":"2024-08-23T07:44:52","modified_gmt":"2024-08-23T05:44:52","slug":"sindaktiliya-tip-1","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/syndactylism-tip-1\/","title":{"rendered":"Syndactyly Type 1"},"content":{"rendered":"
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Syndactyly Type 1 is a congenital disorder characterized by the fusion of two or more fingers or toes, which can lead to limited functionality of the limbs. This condition can manifest itself in varying degrees of severity - from partial fusion to complete absence of interphalangeal septa. Syndactyly can be an isolated disease or combined with other developmental anomalies. This anomaly is most often detected in newborns and can be either unilateral or bilateral in nature. It is important to note that syndactyly most often does not have a significant impact on the general health of the patient, but it can affect his psychoemotional state and quality of life, in particular, due to the social aspects of perception of appearance.<\/p>\n

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