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Oct 12, 2022 · Edwards syndrome, or trisomy 18, is a rare genetic condition where a person has three copies of chromosome 18. It can cause severe intellectual disability, low birth weight, heart issues, and other complications. Learn more about the diagnosis, treatment, and outlook of this condition.
Edwards syndrome is a genetic condition that causes serious health problems and disabilities. It's caused by an extra copy of chromosome 18. Edwards syndrome is very rare. About 1 in 5000 babies has Edwards syndrome. Sadly, most babies with this condition die before or soon after birth.
Dec 13, 2021 · Edwards syndrome is a severe genetic condition that causes physical growth delays, multiple birth defects and intellectual disabilities. Learn about the causes, symptoms, diagnosis and treatment of this rare disorder that affects 1 in 5,000 to 6,000 live births.
Mar 20, 2023 · Edwards syndrome, also called trisomy 18 syndrome, is an autosomal chromosomal disorder due to an extra copy of chromosome 18. Edwards syndrome is one of the autosomal trisomy syndrome, second in frequency only to trisomy 21.
Trisomy 18, also called Edwards syndrome, is a chromosomal condition with abnormalities in many parts of the body. Learn about symptoms, inheritance, genetics and resources for this condition.
Feb 28, 2024 · Trisomy 18, also known as Edwards syndrome, is a chromosome disorder that often results in stillbirth or the early death of an infant.
Trisomy 18, also known as Edwards syndrome, is a genetic disorder caused by the presence of a third copy of all or part of chromosome 18. [3] . Many parts of the body are affected. [3] . Babies are often born small and have heart defects. [3] .
