У нас вы можете посмотреть бесплатно (EN) 6 Fingers or Toes, About Hexadactylism | Nature Facts | ALYYLA Facts или скачать в максимальном доступном качестве, видео которое было загружено на ютуб. Для загрузки выберите вариант из формы ниже:
Если кнопки скачивания не
загрузились
НАЖМИТЕ ЗДЕСЬ или обновите страницу
Если возникают проблемы со скачиванием видео, пожалуйста напишите в поддержку по адресу внизу
страницы.
Спасибо за использование сервиса ClipSaver.ru
6 Fingers or Toes, About Hexadactylism, Nature Facts. Hexadactylism, also known as polydactyly, is a rare medical condition in which an individual is born with six fingers or six toes on one or both hands and feet. This condition affects about 1 in 700-1000 births and is typically caused by a genetic mutation during fetal development. In this video, we will explore the various aspects of hexadactylism, including its causes, symptoms, treatment, and historical and cultural significance. The word hexadactylism is derived from the Greek words "hexa" meaning six and "daktylos" meaning finger or toe. This condition can occur on one or both hands and feet, and the extra digits can be fully formed or incomplete. In some cases, the extra digits may even have bones, muscles, and tendons, making them functional and useful. Hexadactylism can be categorized into three types: preaxial, postaxial, and central. Preaxial hexadactylism is the most common type and involves an extra digit on the thumb side of the hand or the big toe side of the foot. Postaxial hexadactylism involves an extra digit on the pinky side of the hand or the little toe side of the foot. Central hexadactylism involves an extra digit in the middle of the hand or foot. Although hexadactylism is typically harmless and does not cause any functional problems, in some cases, it may be associated with other medical conditions such as syndactyly (fusion of fingers or toes) or cleft hand or foot. It can also lead to social and psychological challenges due to the physical difference. The causes of hexadactylism can vary, and it can be an inherited genetic condition or a result of a spontaneous genetic mutation. In some cases, it may be associated with other genetic disorders such as Down syndrome or Ellis-van Creveld syndrome. Prenatal exposure to certain drugs or chemicals may also increase the risk of hexadactylism. Treatment options for hexadactylism depend on the severity of the condition and the individual's specific needs. In some cases, surgery may be recommended to remove the extra digits or fuse them together. In other cases, physical therapy or occupational therapy may be useful to help the individual adapt to their condition and improve their overall function. In many cultures and throughout history, hexadactylism has been viewed as a sign of good luck or a divine blessing. In some cultures, individuals with hexadactylism are revered for their unique abilities or artistic talents. In the modern era, hexadactylism has become a source of inspiration for artists, musicians, and writers who explore the themes of difference, diversity, and identity. In conclusion, hexadactylism is a rare and fascinating condition that affects a small percentage of the population. While it may present some challenges for those affected, it is often viewed as a source of uniqueness and creativity. By understanding the causes, symptoms, and treatment options for hexadactylism, we can appreciate the diversity of human anatomy and the complexities of genetic variation. Make very sure you Like, Share, and Subscribe to our channel (ALYYLA-Facts) for more informative and interesting videos based on amazing factual facts if you found the information in these video useful. ----- ----- ----- / @alyyla-facts (@alyyla-facts) Facts by ALYYLA: https://alyyla.com/vlogging.html ALYYLA Support: https://alyyla.com/support.html ALYYLA: https://alyyla.com ALYYLA @ Google: https://g.page/ALYYLA ALYYLA @ Linkedin: / alyyla ALYYLA @ Facebook: / alyylasolutions ALYYLA @ Instagram: / alyylasolutions ALYYLA @ Twitter: / alyylasolutions ALYYLA @ Pinterest: / alyylasolutions ----- ----- -----