:: Volume 6, Number 1 (Int J Mol Cell Med 2017) ::
Back to browse issues page Int J Mol Cell Med 2017, 6(1): 61-65
Prenatal Diagnosis of Mosaic Tetrasomy 18p in a Case without Sonographic Abnormalities
Javad Karimzad Hagh1, Thomas Liehr2, Hamid Ghaedi3, Mir Majid Mossalaeie1, Shohreh Alimohammadi4, Faegheh Inanloo Hajiloo1, Zahra Moeini1, Sadaf Sarabi1, Davood Zare-Abdollahi *5
1- Parseh Pathobiology & Genetics Laboratory, Tehran, Iran., Parseh Pathobiology & Genetics Laboratory, Tehran, Iran.
2- Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Jena, Germany., Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Jena, Germany.
3- Department of medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Department of medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
4- Endometrium and Endometriosis Research Center, Faculty of Medicine, Hamedan University of Medical Sciences, Hamedan, Iran., Endometrium and Endometriosis Research Center, Faculty of Medicine, Hamedan University of Medical Sciences, Hamedan, Iran.
5- Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. , D.zareabdollahi@sbmu.ac.ir
Abstract:   (808 Views)

Small supernumerary marker chromosomes (sSMC) are still a major problem in clinical cytogenetics as they cannot be identified or characterized unambiguously by conventional cytogenetics alone. On the other hand, and perhaps more importantly in prenatal settings, there is a challenging situation for counseling how to predict the risk for an abnormal phenotype, especially in cases with a de novo sSMC. Here we report on the prenatal diagnosis of a mosaic tetrasomy 18p due to presence of an sSMC in a fetus without abnormal sonographic signs. For a 26-year-old, gravida 2 (para 1) amniocentesis was done due to consanguineous marriage and concern for Down syndrome, based on borderline risk assessment. Parental karyotypes were normal, indicating a de novo chromosome aberration of the fetus. FISH analysis as well as molecular karyotyping identified the sSMC as an i(18)(pter->q10::q10->pter), compatible with tetrasomy for the mentioned region. Cordocentesis was done due to normal sonography and the results from amniocentesis were confirmed. The parents opted for pregnancy termination and post mortem examination now noted, low anterior hairline, large philtrum, low-set posteriorly rotated malformed ears with prominent antihelix, lower limbs joint contracture and digital anomalies, including long and narrow toes with clinodactyly of the 1st and 5th toes and postaxial polydactyly of one hand. De novo i(18p) can be considered as a special case in the sense that the major relevant phenotypes mentioned for it, i.e. feeding difficulties, abnormalities in muscle tone and developmental/mental retardation, cognitive and behavioral characteristics, recurrent otitis media and seizures, are mostly postnatal. This emphasizes the necessity to determine the nature of a de novo euchromatic marker chromosome, especially in cases with normal ultrasound result and the suitability of a cordocentesis in order to better predicting the pregnancy outcome and parental counseling.

Keywords: Tetrasomy, prenatal, cordocentesis, amniocentesis, polydactyly, isochromosome 18p, marker, small supernumerary marker chromosome (sSMC)
Full-Text [PDF 1304 kb]   (288 Downloads)    
Type of Study: Case Report | Subject: Genetics & Disease
Received: 2016/08/15 | Accepted: 2016/10/22 | Published: 2017/01/17



DOI: 10.22088/acadpub.BUMS.6.1.61


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Back to browse issues page Volume 6, Number 1 (Int J Mol Cell Med 2017)