|Coincidence of trisomy 18 and robertsonian (13; 14).|
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|PMID: 23113216 Owner: NLM Status: PubMed-not-MEDLINE|
|This case report presents a coincidence of trisomy 18 and balanced Robertsonian translocation (13;14). Aneuploidy was suspected based on anomalies detected in ultrasound scan and confirmed with karyotype. In a 31 years-old healthy woman with a history of one miscarriage, second trimester ultrasound scan reported IUGR (<3rd percentile) with normal amniotic fluid, bilateral choroid plexus cysts, suspicious agenesis of corpus callosum and clenched hands. Amniocentesis was performed and karyotype was 46xx,der(13;14) (q10;q10),+18. Maternal karyotype was 45xx,der(13;14)(q10;q10). Pregnancy was continued due to legal limitation for termination after 20 weeks gestation. Delivery was done at 36 weeks gestation. A female newborn was borned and a physical feature was hypotonia, small mouth, prominent occiput, low-set and posteriorly rotated ears, clenched hands with overlapping fingers and rocker bottom feet. Ultrasound scan and echocardiography detected agenesis of corpus callosum and VSD, ASD, PDA and cardiomegaly. These features are typical of trisomy 18. Balanced Robertsonian translocation usually has no phenotypic expression. Genetic counseling and prenatal diagnosis for future pregnancy was recommended.|
|A Jamal; S Mousavi; A Alavi|
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|Type: Journal Article Date: 2012-07-31|
|Title: Iranian journal of public health Volume: 41 ISSN: 2251-6085 ISO Abbreviation: Iran. J. Public Health Publication Date: 2012|
|Created Date: 2012-10-31 Completed Date: 2012-11-01 Revised Date: 2013-02-19|
Medline Journal Info:
|Nlm Unique ID: 7505531 Medline TA: Iran J Public Health Country: Iran|
|Languages: eng Pagination: 91-3 Citation Subset: -|
|Dept. of OB/GYN, Perinatology Division, Shariati Hospital, Tehran university of Medical Sciences, Tehran, Iran.|
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Journal ID (nlm-ta): Iran J Public Health
Journal ID (iso-abbrev): Iran. J. Public Health
Journal ID (publisher-id): IJPH
Publisher: Tehran University of Medical Sciences
Copyright © Iranian Public Health Association & Tehran University of Medical Sciences
Received Day: 28 Month: 12 Year: 2011
Accepted Day: 18 Month: 5 Year: 2012
Electronic publication date: Day: 31 Month: 7 Year: 2012
collection publication date: Year: 2012
Volume: 41 Issue: 7
First Page: 91 Last Page: 93
PubMed Id: 23113216
Publisher Id: ijph-41-91
|Coincidence of Trisomy 18 and Robertsonian (13; 14)|
|Dept. of OB/GYN, Perinatology Division, Shariati Hospital, Tehran university of Medical Sciences, Tehran, Iran
|*Corresponding Author: E-mail address: email@example.com
Chromosomal abberations include two broad categories: numerical and structural anomalies. Trisomy 18 is the second most common autosomal trisomy, also known as Edward syndrome, is a well-known human aneuploidy with a short life time expectancy. It has an overall frequency of 1 in 3000 up to 1 in 8000 newborns, 3 to 4 times more common in females than in males (1), and is a maternal age related trisomy (2).
Robertsonian translocation (Rob) is centric fusion of two acrocentric chromosomes, and is the most common chromosomal translocation, occurs 1 per 1000 in general population. The most common Rob is between chromosomes 13 and 14 (13q;14q) which constitutes 75% of all Robs. As long as the fused q arms are intact, the Rob carriers are usually phenotypically normal (3). However unbalanced gametes of heterozygous carriers are common and give rise to monosomic or trisomic fetuses. Most monosomies and trisomies are lethal and spontaneously are lost early in pregnancy (4). Observed incidence of normal/balanced offspring is 13.28% (5). Coincidence of Rob(13;14) with trisomy 18 has been reported as denovo event (6) or in offspring of Rob carriers, both are rare conditions. This rather uncommon observation has been interpreted as interchromosomal effect (ICE), which lead to missegregation of the chromosomes not involved in the translocation. The issue is still very controversial (7–8).
Ultrasound findings, maternal serum markers, and parental risk factors for genetic disease are all considered in determining the risk that the fetus is affected. Fetal karyotyping is suggested when structural anomalies or early intrauterine growth retardation,IUGR (weight below the 10th percentile for gestational age) is detected (9).
A 31 years-old healthy mother, gravid 2 and 1 miscarriage (blighted ovum), her mother had an intrauterine fetal demise without gross anomaly. The father was 30 years-old and healthy, family history was unremarkable. Second trimester screening quadruple test result was low risk for trisomy 18, 21 and 13. However, ultrasound scan at 22 week’s gestation revealed a single alive fetus with symmetric IUGR <3%, normal amniotic fluid. Fetal anomaly scan demonstrated: bilateral choroid plexus cysts (8–10 millimeters), suspicious agenesis of corpus callosum and clenched hands. She was referred to our unit for karyotyping. An amniocentesis was performed at 22 weeks gestation. Amniocytes were cultured using standard techniques, finding on GTG-banded metaphase spreads showed a karyotype of 46xx, der(13;14)(q10;q10),+18, trisomy 18 and balanced Robertsonian translocation between nonhomologous acrocentric chromosomes 13 and 14. Karyotypes of parents were requested. Father’s was normal and mother’s was described as 45xx,der(13;14)(q10;q10) (Fig. 1).
Following genetic counseling and informing of poor prognosis for fetus with Edward syndrome, mother chose to terminate the pregnancy but because of legal limitations after 20 weeks gestation, pregnancy was continued. A female infant was delivered in 36 weeks gestation. She weighed 2000 grams (<3rd percentile), length was 43 centimeters, (<3rd percentile) and head circumference was 31.5 centimeters (10–50th percentile). Physical findings were hypotonia, small mouth, prominent occiput, low-set and posteriorly rotated ears, clenched hands with overlapping fingers and rocker bottom feet. Brain ultrasound scan showed agenesis of corpus callosum and echocardiography reported VSD, ASD, PDA, and cardiomegaly.
She was physically retarded and had problems such as failure to thrive, feeding difficulties, and frequent NICU admissions. She died at 11 months-old.
Robs usually have reproductive risks, as our case had a previous miscarriage and a recent pregnancy with aneuploidy A range of 77 to 97% fetuses with trisomy 18 has been detected during second trimester ultrasound (10). Detection rate depends on gestational age, operator’s expertise, and ultrasound machine quality. In our case, aneuploidy was suspected in ultrasound scan, and a rare complex chromosomal aberration of Rob (13;14) and trisomy 18, was diagnosed by karyotype.
The major phenotypic features of the newborn were characteristic of trisomy 18. Balanced Rob usually does not have phenotypic consequences because the lost sections of acrocentric chromosomes do not contain unique genetic sequences. Trisomy 18 cases are usually caused by primary nondisjunction in maternal meiosis II (11). It is postulated that translocations disturb meiotic disjunction. Interchromosomal effect maybe exists, as several reports suggest a higher rate of chromosome abnormalities in Robs (8).
Genetic counseling and consideration of prenatal diagnosis is recommended for families with chromosomal translocations and reproductive failures (7, 8). Although second trimester genetic ultrasound scan is helpful for detection of aneuploidies, first trimester screening has improved detection rate and should be offered to all pregnant women (12), for early detection and safe and legal termination.
Ethical issues (Including plagiarism, Informed Consent, misconduct, data fabrication and/or falsification, double publication and/or submission, redundancy, etc) have been completely observed by the authors.
The authors declare that there is no conflict of interests.
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Keywords: Robertsonian translocation, Trisomy 18, Prenatal diagnosis, Interchromosomal effect.
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