Trisomy 18 is a genetic disorder associated with the presence of extra material from chromosome 18.
Trisomy 18 is a relatively common syndrome affecting approximately 1 out of 3,000 live births. It is three times more common in girls than boys. The syndrome is caused by the presence of an extra material from chromosome 18. The extra material interferes with normal development.
- Clenched hands
- Crossed legs (preferred position)
- Heart disease (congenital)
- Hole, split, or cleft in the iris (coloboma)
- Kidney problems
- Low birth weight
- Low-set ears
- Mental deficiency
- Separation between the left and right side of the rectus abdominis muscle (diastasis recti)
- Small head (microcephaly)
- Small jaw (micrognathia)
- Umbilical hernia or inguinal hernia
- Underdeveloped fingernails
- Undescended testicle
- Unusual shaped chest (Pectus carinatum)
Examination of the pregnant woman may show an unusually large uterus and extra amniotic fluid. An unusually small placenta may be seen when the baby is born.
There are often signs of congenital heart disease, such as:
Tests may also show kidney problems, including:
Medical management of children with Trisomy 18 is planned on a case-by-case basis and depends on the individual circumstances of the patients
Fifty percent of infants with this condition do not survive beyond the first week of life. Some children have survived to teenage years, but with serious medical and developmental problems.
Complications depend on the specific defects and symptoms.
Prenatal diagnosis of trisomy 18 is possible with an amniocentesis or chorionic villus sampling and chromosome studies on amniotic cells. Parents who have a child with translocational trisomy 18 and want additional children should have chromosome studies, because they are at increased risk to have another child with trisomy 18.
(Referrence from MedlinePlus Medical Encyclopedia)
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