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Dec 13, 2021 · Edwards syndrome is a severe genetic condition that causes multiple birth defects and low life expectancy. Learn about the symptoms, causes, diagnosis and treatment of this condition and how it affects your child's development and growth.
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.
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.
Feb 28, 2024 · Trisomy 18 is a chromosome disorder that causes many serious health problems and physical defects in babies. Learn about the types, risk factors, diagnosis, treatment, and life expectancy of trisomy 18.
Edwards' syndrome is a rare and serious condition caused by having 3 copies of chromosome 18. It affects how long a baby may survive and can cause learning disability, physical features and health problems.
Trisomy 18, also called Edward syndrome, is a genetic condition that causes many life-limiting symptoms. Learn about the causes, types, diagnosis and treatment options for trisomy 18 from Cincinnati Children's Hospital Medical Center.
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.
