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Trisomy 18 is a chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 18th chromosome, either in whole (trisomy 18) or in part (such as ?Trisomy 18 is a serious genetic condition that occurs when there are three copies of chromosome 18 instead of the usual two. Learn about symptoms, diagnosis and outlook.+Edwards syndrome (trisomy 18) is a genetic condition where three cells attach to chromosome 18, causing growth delays that can be life-threatening.,Feb 28, 2024 · Trisomy 18 is a condition where you have three copies of each chromosome 18 in your bodys cells instead of two. This can lead to serious physical and mental disabi-Trisomy 18 is caused by genetic mutations, also known as pathogenic variants. Genetic mutations can be hereditary, when parents pass them down to their children, or they may occur $Trisomy 18, also called Edwards syndrome, is a chromosomal condition associated with abnormalities in many parts of the body. Individuals with trisomy 18 often have slow growth …^Find out about Edwards’ syndrome (trisomy 18) including the symptoms, types, how its diagnosed and what causes it.


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