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Ectrosyndactyly is a complex medical term that refers to a rare congenital condition characterized by the fusion of fingers or toes and the absence or malformation of certain digits. This condition affects the limbs and can manifest in various ways, making it an essential topic of discussion in the realms of medical genetics and orthopedic surgery.
The term "ectrosyndactyly" is derived from two Greek words: "ektroma," meaning "abortive" or "to cut off," and "syndaktylia," which refers to the fusion of digits. Thus, the term encompasses both aspects of the condition—the loss or malformation of digits combined with their abnormal fusion.
Ectrosyndactyly is often seen in conjunction with other congenital syndromes, notably the well-known "Ectrodactyly" syndrome, which involves a more extensive absence of digits along with abnormal hand or foot structure. This association with various syndromes emphasizes the importance of thorough genetic investigation and screening for affected individuals.
Here are some key features and facts about ectrosyndactyly:
In summary, ectrosyndactyly is a distinctive congenital condition marked by the fusion and absence of digits. Its complexity necessitates a multidisciplinary approach for effective diagnosis and treatment. With ongoing research, advancements in genetic understanding and surgical techniques continue to improve the outlook for individuals affected by this condition, ensuring they can lead productive and fulfilling lives despite the challenges they face.
проектирование частного дома под ключ