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Dec 13, 2021 · Edwards syndrome, also known as trisomy 18, is a very severe genetic condition that affects how your child’s body develops and grows. Children diagnosed with trisomy 18 have a low birth weight, multiple birth defects and defining physical characteristics.
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. Many parts of the body are affected. Babies are often born small and have heart defects.
Edwards syndrome is a rare genetic condition caused by an extra copy of chromosome 18. It causes serious health problems and disabilities and most babies with this condition die before or soon after birth.
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.
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 complications, such as intellectual disability, heart issues, and low birth weight. Learn more about the diagnosis, treatment, and outlook of this condition.
Edwards' syndrome is a rare and serious condition caused by an extra chromosome 18. Learn about the types, symptoms, screening, diagnosis and treatment of this condition.
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.
