Search results
Results From The WOW.Com Content Network
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 is a condition where you have three copies of each chromosome 18 in your body's cells instead of two. This can lead to serious physical and mental disabilities.
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 due to translocations).
Trisomy 18 is a rare genetic disorder that affects approximately 1 in every 3,315 births in the United States — around 1,187 babies each year. In typical development, a baby gets 23 pairs of...
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 before birth (intrauterine growth retardation) and a low birth weight.
Trisomy 18 is a chromosome disorder characterized by having 3 copies of chromosome 18 instead of the usual 2 copies. Signs and symptoms include severe intellectual disability; low birth weight; a small, abnormally shaped head; a small jaw and mouth; clenched fists with overlapping fingers; congenital heart defects; and various abnormalities of ...
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.
Trisomy 18 is a rare chromosomal disorder in which all or a critical region of chromosome 18 appears three times (trisomy) rather than twice in cells of the body. In some children, trisomy 18 may be present in only a percentage of cells, whereas other cells contain the typical chromosomal pair (mosaicism).
Edwards' syndrome, also known as trisomy 18, is a serious genetic condition caused by an additional copy of chromosome 18 in some or all of the cells in the body.
Trisomy 18 caused by an extra chromosome 18. Infants are typically small and have many physical abnormalities and problems with internal organs. Tests can be done before or after birth to confirm the diagnosis.