>
Fa   |   Ar   |   En
   Prenatal Diagnosis of Mosaic Tetrasomy 18p in A Case Without Sonographic Abnormalities  
   
نویسنده Karimzad Hagh Javad ,Liehr Thomas ,Ghaedi Hamid ,Mossalaeie Mir Majid ,Alimohammadi Shohreh ,Inanloo Hajiloo Faegheh ,Moeini Zahra ,Sarabi Sadaf ,Zare-Abdollahi Davood
منبع International Journal Of Molecular And Cellular Medicine - 2017 - دوره : 6 - شماره : 1 - صفحه:61 -65
چکیده    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.
کلیدواژه Tetrasomy ,Prenatal ,Cordocentesis ,Amniocentesis ,Polydactyly ,Isochromosome 18p ,Marker ,Small Supernumerary Marker Chromosome (Ssmc)
آدرس Parseh Pathobiology & Genetics Laboratory, ایران, Friedrich Schiller University, Jena University Hospital, Institute Of Human Genetics, Germany, Shahid Beheshti University Of Medical Sciences, Faculty Of Medicine, Department Of Medical Genetics, ایران, Parseh Pathobiology & Genetics Laboratory, ایران, Hamedan University Of Medical Sciences, Endometrium And Endometriosis Research Center, Faculty Of Medicine, ایران, Parseh Pathobiology & Genetics Laboratory, ایران, Parseh Pathobiology & Genetics Laboratory, ایران, Parseh Pathobiology & Genetics Laboratory, ایران, University Of Social Welfare And Rehabilitation Sciences, Genetics Research Center, ایران
پست الکترونیکی d.zareabdollahi@sbmu.ac.ir
 
     
   
Authors
  
 
 

Copyright 2023
Islamic World Science Citation Center
All Rights Reserved