Health Encyclopedia

Trisomy 18

Definition

Trisomy 18 is a genetic disorder in which a person has a third copy of genetic material from chromosome 18, instead of the usual two copies.

Alternative Names

Edwards syndrome

Causes, incidence, and risk factors

Trisomy 18 is a relatively common syndrome. It is three times more common in girls than boys. The syndrome is caused by the presence of extra material from chromosome 18. The extra material interferes with normal development.

Symptoms

Clenched hands
Crossed legs (preferred position)
Feet with a rounded bottom (rocker-bottom feet)
Low birth weight
Low-set ears
Mental deficiency
Small head (microcephaly)
Small jaw (micrognathia)
Underdeveloped fingernails
Undescended testicle
Unusual shaped chest (pectus carinatum)

Signs and tests

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.

Physical examination of the infant may show unusual fingerprint patterns. X-rays may show a short breast bone. Chromosome studies show trisomy 18, partial trisomy, or translocation.

Other signs include:

Hole, split, or cleft in the iris (coloboma)
Separation between the left and right side of the rectus abdominis muscle (diastasis recti)
Umbilical hernia or inguinal hernia

There are often signs of congenital heart disease, such as:

Tests may also show kidney problems, including:

Treatment

Treatment of children with Trisomy 18 is planned on a case-by-case basis. Which treatments are used depends on the patient's individual condition.

Support Groups

Support Organization for Trisomy 18, 13 and Related Disorders (SOFT) - www.trisomy.org
Trisomy 18 Foundation - www.trisomy18.org

Expectations (prognosis)

Fifty percent of infants with this condition do not survive beyond the first week of life. Some children have survived to the teenage years, but with serious medical and developmental problems.

Complications

Complications depend on the specific defects and symptoms.

Calling your health care provider

Call your health care provider and genetic counselor if you have had a child with Trisomy 18 and you plan to have another child. Genetic counseling can help families understand the condition, the risks of inheriting it, and how to care for the patient.

Prevention

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 of having another child with Trisomy 18.

Review Date:8/11/2009
Reviewed By:Diana Chambers, MS, EdD, Certified Genetics Counselor (ABMG), Charter Member of the ABGC, University of Tennessee, Memphis, TN. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.

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