Health Encyclopedia

Trisomy 13

Definition

Trisomy 13, also called Patau syndrome, is a genetic disorder associated with the presence of extra material from chromosome 13.

Alternative Names

Patau syndrome

Causes, incidence, and risk factors

Trisomy 13 occurs when extra DNA from chromosome 13 appears in some or all of the body's cells.

Trisomy 13 -- the presence of an extra (third) chromosome 13 in all of the cells.
Trisomy 13 mosaicism -- the presence of an extra chromosome 13 in some of the cells.
Partial trisomy -- the presence of a part of an extra chromosome 13 in the cells.

The extra material interferes with normal development.

Trisomy 13 occurs in about 1 out of every 10,000 newborns. Most cases are not passed down through families (inherited). Instead, the events that lead to Trisomy 13 occur in either the sperm or the egg that forms the fetus.

Symptoms

Cleft lip or palate
Close-set eyes -- eyes may actually fuse together into one
Decreased muscle tone
Extra fingers or toes (polydactyly)
Hernias: umbilical hernia, inguinal hernia
Hole, split, or cleft in the iris (coloboma)
Low-set ears
Mental retardation, severe
Scalp defects (absent skin)
Seizures
Single palmar crease
Skeletal (limb) abnormalities
Small eyes
Small head (microcephaly)
Small lower jaw (micrognathia)
Undescended testicle (cryptorchidism)

Signs and tests

The infant may have a single umbilical artery at birth. There are often signs of congenital heart disease, such as:

Abnormal placement of the heart toward the right side of the chest instead of the left
Atrial septal defect
Patent ductus arteriosus
Ventricular septal defect

Gastrointestinal x-rays or ultrasound may show rotation of the internal organs.

MRI or CT scans of the head may reveal a problem with the structure of the brain. The problem is called holoprosencephaly. It is the joining together of the two sides of the brain.

Chromosome studies show trisomy 13, trisomy 13 mosaicism, or partial trisomy.

Treatment

Medical management of children with Trisomy 13 is planned on a case-by-case basis and depends on the individual circumstances of the patient.

Support Groups

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

Living with Trisomy 13 -- www.livingwithtrisomy13.org

Expectations (prognosis)

The syndrome involves multiple abnormalities, many of which are not compatible with life. More than 80% of children with trisomy 13 die in the first month.

Complications

Complications begin almost immediately. Congenital heart disease is present in approximately 80% of infants with Trisomy 13. Complications may include:

Breathing difficulty or lack of breathing (apnea)
Deafness
Feeding problems
Heart failure
Seizures
Vision problems

Calling your health care provider

Call for an appointment with your health care provider if you have had a child with Trisomy 13, and you plan to have another child.

Prevention

Trisomy 13 can be diagnosed prenatally by amniocentesis with chromosome studies of the amniotic cells.

Parents of infants with trisomy 13 caused by a translocation should have genetic testing and counseling, which may help them prevent recurrence.

Review Date:7/1/2007
Reviewed By:Brian Kirmse, MD, Mount Sinai School of Medicine, Department of HumanGenetics, New York, NY. Review provided by VeriMed Healthcare Network.

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