Patau's Syndrome (Trisomy 13)

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Synonym: trisomy 13

Patau's syndrome (trisomy 13) carries a high mortality rate with multiple congenital abnormalities which result in severe physical and mental impairment.

  • It is usually due to a free-standing trisomy with an extra number 13 chromosome, instead of the usual pair, in all cells. 
  • An unbalanced chromosome translocation can also occur - commonly, a Robertsonian translocation. This is when an extra copy of chromosome 13 is attached to another chromosome.
  • There may also be mosaic variations in which some cells are normal with 46 chromosomes and others have the extra chromosome. Infants with mosaic variations tend to be less severely affected.

The prevalence of trisomy 13 is between 1 in 5,000 and 1 in 29,000 live births, which is the third most common autosomal trisomy in newborns after trisomy 21 and trisomy 18.[1] 

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  • A personal or close family history of giving birth to an affected child increases the risk.
  • Risk rises with increasing maternal age but not as markedly as with Down's syndrome (trisomy 21) or Edwards' syndrome (trisomy 18).[2]

Many fetuses never survive until term and are stillborn or spontaneously abort. Features include:

  • Intrauterine growth restriction and low birth weight.
  • Congenital heart defects: these occur in 80%; they include atrial septal defect, ventricular septal defect, patent ductus arteriosus, dextrocardia.
  • Holoprosencephaly: the brain doesn't divide into two halves; this can present with midline facial defects including:
    • Cleft lip and palate.
    • Microphthalmia or anophthalmia.
    • Nasal malformation.
    • Hypotelorism (reduced distance between the eyes) or cyclops.
  • Other brain and central nervous system abnormalities including:
    • Neural tube defects.
    • Other anatomical defects of the brain
    • Severe learning disability.
    • Problems with control of breathing (central apnoea).
  • Other craniofacial abnormalities include:
    • Microcephaly.
    • Scalp defects (cutis aplasia: skin missing from the scalp).
    • Ear malformations and deafness.
    • Capillary haemangiomata.
  • Gastrointestinal abnormalities: omphalocele, exomphalos, hernias.
  • Urogenital malformations: polycystic kidneys, micropenis or hypertrophy of the clitoris.
  • Abnormalities of hands and feet: polydactyly (extra fingers or toes), rocker-bottom feet.
  • Infants with Patau's syndrome and Edwards' syndrome can have similar features and be difficult to differentiate.
  • Cytogenetic studies and chromosomal analysis will confirm the diagnosis.
  • Organ systems will need specific investigation depending on the abnormality - eg, echocardiography for cardiac abnormalities; skeletal radiography, etc.
  • Treatment of a 'liveborn' infant is generally supportive but life-sustaining measures are not always carried out. Considerable thought and discussion are recommended before undertaking measures such as surgical correction of abnormalities. Nasogastric or gastrostomy feeding is feasible but the clinician should take into account the wishes of the parents and any potential harms it may cause the infant.
  • Parents will need a great deal of support and counselling.
  • If Patau's syndrome is due to an unbalanced chromosome translocation or structural chromosomal abnormality, both parents should undergo chromosomal analysis. It may be that the translocation in the infant occurred de novo but a balanced translocation may be found in one of the parents. This has significance for future pregnancies because of a higher risk of recurrence. Other family members may also be affected.
  • Screening and/or prenatal diagnosis should be offered for future pregnancies. Women who have had a previous trisomic pregnancy, especially those under 35 years of age at the time, appear to be at an increased risk of future pregnancies being trisomic.[4] 
  • Life expectancy is very limited. Median survival is 2.5 days.
    • About 50% live longer than 1 week.
    • 5-10% of infants live longer than 1 year.
  • Profound mental retardation and developmental delay occur in survivors. Seizures and feeding difficulties are common.
  • Specific ultrasound findings may suggest trisomy 13 and subsequent cytogenetic studies may therefore be indicated. Findings include increased nuchal translucency, cardiac defects, neural tube defects, facial clefting, renal abnormalities and omphalocele
  • A study from Kings College Hospital showed that at the 11- to 13(+6)-week scan, the measurement of fetal nuchal translucency and fetal heart rate and fetal examination for holoprosencephaly, exomphalos, and megacystis can identify > 90% of fetuses with trisomy 13.[6]
  • First-trimester multiple marker screening (that which is currently offered for Down's syndrome screening) may also help to identify a fetus with trisomy 13 or 18. Markers can include maternal age, nuchal translucency measurement, pregnancy-associated plasma protein A (PAPPA) and human chorionic gonadotrophin (hCG). Ultrasound at that time may also show fetal anomalies.
  • Second-trimester screening tests can be offered if the mother presents later. See the separate article Antenatal Screening for Down's Syndrome for more details about second-trimester screening tests.
  • In a UK-based study from 2003, 44 cases of trisomy 13 and 88 cases of trisomy 18 were examined. 64% were first detected by chromosomal analysis because of abnormalities noted on fetal anomaly scanning in the second trimester. 3% of cases were detected through the serum screening programme currently offered for Down's syndrome. 11% of cases were detected postnatally. Of note, in the same study, 12% of couples chose to continue with the pregnancy after prenatal diagnosis.[2]
  • Amniocentesis or chorionic villus sampling is needed to make a definitive prenatal diagnosis.
  • Cytogenetic study of fetal blood may also be carried out.
  • Mothers over the age of 35 may choose to go straight to diagnostic testing. Others mothers may choose to have diagnostic testing after a positive screening test.
  • Klaus Patau was a German-born, American human geneticist. Patau et al described the syndrome in 1960.[7]
  • The clinical appearance of trisomy 13 was first described by Erasmus Bartholin in 1657 but he was unaware of the aetiology.

Further reading & references

  1. Tsukada K, Imataka G, Suzumura H, et al; Better prognosis in newborns with trisomy 13 who received intensive treatments: a retrospective study of 16 patients. Cell Biochem Biophys. 2012 Jul;63(3):191-8. doi: 10.1007/s12013-012-9355-0.
  2. Parker MJ, Budd JL, Draper ES, et al; Trisomy 13 and trisomy 18 in a defined population: epidemiological, genetic and prenatal observations.; Prenat Diagn. 2003 Oct;23(10):856-60.
  3. Plaiasu V, Ochiana D, Motei G, et al; Clinical relevance of cytogenetics to pediatric practice. Postnatal findings of Patau syndrome - Review of 5 cases. Maedica (Buchar). 2010 Jul;5(3):178-85.
  4. De Souza E, Halliday J, Chan A, et al; Recurrence risks for trisomies 13, 18, and 21. Am J Med Genet A. 2009 Dec;149A(12):2716-22. doi: 10.1002/ajmg.a.33099.
  5. Chitayat D, Langlois S, Wilson RD; Prenatal screening for fetal aneuploidy in singleton pregnancies. J Obstet Gynaecol Can. 2011 Jul;33(7):736-50.
  6. Papageorghiou AT, Avgidou K, Spencer K, et al; Sonographic screening for trisomy 13 at 11 to 13(+6) weeks of gestation. Am J Obstet Gynecol. 2006 Feb;194(2):397-401.
  7. Patau K, Smith DW, Therman E, et al; Multiple congenital anomaly caused by an extra autosome.; Lancet. 1960 Apr 9;1:790-3.

Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. EMIS has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.

Original Author:
Dr Michelle Wright
Current Version:
Peer Reviewer:
Dr Adrian Bonsall
Last Checked:
28/03/2013
Document ID:
2578 (v24)
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