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Trisomy 18, also known as Edwards syndrome, named after the British physician John Hilton Edwards, who first described the condition in 1960, is a genetic condition characterized by the presence of an extra chromosome 18 in some or all of the body's cells. This additional genetic material disrupts normal development, leading to a range of physical and intellectual disabilities. In this article, we delve into the intricacies of trisomy 18, exploring its causes, symptoms, diagnosis, management, and the impact it has on affected individuals and their families.
In this video, we will explore the different types of trisomy, their causes, symptoms, diagnosis, treatment and prevention options, and address frequently asked questions.
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Chapter:
00:00 Trisomy 18 (Edwards syndrome)
00:48 Causes of Trisomy 18 (Edwards syndrome)
01:58 Symptoms and Signs
03:16 Diagnosis and Prenatal Screening
04:41 Treatment and Management idea for trisomy 18
05:16 Prognosis of trisomy 18
05:58 FAQs about Trisomy 18
08:05 Thanks, Please like, comment, and subscribe Anatomy Note YouTube channel
#geneticcondition #genetics #trisomia #trisomy18
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Video credit: Storyblocks
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