Literature DB >> 28868271

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-Abdollahi5.   

Abstract

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.

Entities:  

Keywords:  Tetrasomy; amniocentesis; cordocentesis; isochromosome 18p; marker; polydactyly; prenatal; small supernumerary marker chromosome (sSMC)

Year:  2017        PMID: 28868271      PMCID: PMC5568194     

Source DB:  PubMed          Journal:  Int J Mol Cell Med        ISSN: 2251-9637


  10 in total

1.  Grandmaternal origin of an isochromosome 18p present in two maternal half-sisters.

Authors:  J Boyle; K Sangha; F Dill; W P Robinson; S L Yong
Journal:  Am J Med Genet       Date:  2001-06-01

2.  Tetrasomy 18p: report of cognitive and behavioral characteristics.

Authors:  Louise O'Donnell; Bridgette T Soileau; Courtney Sebold; Jonathan Gelfond; Daniel E Hale; Jannine D Cody
Journal:  Am J Med Genet A       Date:  2015-04-21       Impact factor: 2.802

3.  Tetrasomy 18p de novo: identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typing.

Authors:  T Eggermann; H Engels; B Moskalonek; M M Nöthen; J Müller-Navia; E Schleiermacher; G Schwanitz; S Stengel-Rutkowski
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

4.  The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsy.

Authors:  A Battaglia; F Gurrieri; E Bertini; A Bellacosa; M G Pomponi; M Paravatou-Petsotas; S Mazza; G Neri
Journal:  Neurology       Date:  1997-04       Impact factor: 9.910

5.  Prenatal diagnosis of mosaic tetrasomy 18p.

Authors:  Chih-Ping Chen; Tsang-Ming Ko; Yi-Ning Su; Schu-Rern Chern; Jun-Wei Su; Yu-Ting Chen; Dai-Dyi Town; Wayseen Wang
Journal:  Taiwan J Obstet Gynecol       Date:  2012-12       Impact factor: 1.705

6.  Tetrasomy 18p: report of the molecular and clinical findings of 43 individuals.

Authors:  Courtney Sebold; Elizabeth Roeder; Marsha Zimmerman; Bridgette Soileau; Patricia Heard; Erika Carter; Martha Schatz; W Abraham White; Brian Perry; Kent Reinker; Louise O'Donnell; Jack Lancaster; John Li; Minire Hasi; Annice Hill; Lauren Pankratz; Daniel E Hale; Jannine D Cody
Journal:  Am J Med Genet A       Date:  2010-09       Impact factor: 2.802

7.  Tetrasomy 18p de novo: parental origin and different mechanisms of formation.

Authors:  M Bugge; E Blennow; U Friedrich; M B Petersen; F Pedeutour; A Tsezou; A Orum; S Hermann; T Lyngbye; C Sarri; D Avramopoulos; S Kitsiou; J C Lambert; M Guzda; N Tommerup; K Brøndum-Nielsen
Journal:  Eur J Hum Genet       Date:  1996       Impact factor: 4.246

8.  Isochromosome 18p results from maternal meiosis II nondisjunction.

Authors:  D Kotzot; G Bundscherer; F Bernasconi; L Brecevic; I W Lurie; S Basaran; C Baccicchetti; A Höller; C Castellan; C Braun-Quentin; R A Pfeiffer; A Schinzel
Journal:  Eur J Hum Genet       Date:  1996       Impact factor: 4.246

9.  Complex small supernumerary marker chromosomes - an update.

Authors:  Thomas Liehr; Sanja Cirkovic; Tanja Lalic; Marija Guc-Scekic; Cynthia de Almeida; Jörg Weimer; Ivan Iourov; Maria Isabel Melaragno; Roberta S Guilherme; Eunice-Georgia G Stefanou; Dilek Aktas; Katharina Kreskowski; Elisabeth Klein; Monika Ziegler; Nadezda Kosyakova; Marianne Volleth; Ahmed B Hamid
Journal:  Mol Cytogenet       Date:  2013-10-31       Impact factor: 2.009

10.  A case report of prenatally diagnosed tetrasomy 18p.

Authors:  Phill-Seung Jung; Hye-Sung Won; In-Ji Cho; Min-Kyung Hyun; Jae-Yoon Shim; Pil-Ryang Lee; Ahm Kim
Journal:  Obstet Gynecol Sci       Date:  2013-05-16
  10 in total
  1 in total

1.  Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins-Diagnostic implications.

Authors:  Małgorzata Rydzanicz; Pawel Olszewski; Darek Kedra; Hanna Davies; Natalia Filipowicz; Bozena Bruhn-Olszewska; Marco Cavalli; Krzysztof Szczałuba; Marlena Młynek; Marcin M Machnicki; Piotr Stawiński; Grażyna Kostrzewa; Paweł Krajewski; Dariusz Śladowski; Krystyna Chrzanowska; Jan P Dumanski; Rafał Płoski
Journal:  Mol Genet Genomic Med       Date:  2020-12-14       Impact factor: 2.183

  1 in total

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