Characterization of a de novo Supernumerary Neocentric Ring Chromosome Derived from Chromosome 7

被引:2
|
作者
Louvrier, Camille [1 ]
Egea, Gregory [1 ,5 ]
Labalme, Audrey [1 ]
Des Portes, Vincent [2 ]
Gazzo, Sophie [6 ]
Callet-Bauchu, Evelyne [6 ]
Till, Marianne [1 ]
Sanlaville, Damien [1 ,4 ]
Edery, Patrick [3 ,4 ]
Schluth-Bolard, Caroline [1 ,4 ]
机构
[1] Ctr Biol & Pathol Est, Lab Cytogenet Constitut, Serv Genet, FR-69677 Bron, France
[2] Hosp Civils Lyon, Hop Femme Mere Enfant, Serv Neuropediat, Bron, France
[3] Hosp Civils Lyon, Hop Femme Mere Enfant, Serv Genet, Bron, France
[4] CNRS UMR5292, INSERM U1028, Ctr Rech Neurosci Lyon, TIGER, Lyon, France
[5] Lab Biomnis, Lyon, France
[6] Hosp Civils Lyon, Ctr Hosp Lyon Sud, Hematol Lab, Pierre Benite, France
关键词
Array-CGH; Mosaic; Neocentromere; Small supernumerary marker chromosome; 7q22q31; PARTIAL TRISOMY; MARKER CHROMOSOMES; CYSTIC-FIBROSIS; ARRAY CGH; CENTROMERE; TRANSLOCATION; DUPLICATION; 7Q;
D O I
10.1159/000442265
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Supernumerary ring chromosomes (SRC) are usually derived from regions adjacent to the centromere. Their identification may be challenging, particularly in case of low mosaicism. Here, we report on a patient who was referred for major in utero growth retardation, severe developmental delay, facial dysmorphism, cleft palate, and hypospadias. The karyotype showed a small SRC in mosaic. The combination of FISH, M-FISH and array-CGH was necessary for a complete characterization of this SRC. M-FISH revealed that the SRC originated from chromosome 7. Array-CGH performed with a 400K oligonucleotide array showed a gain in region 7q22.1q31.1 present in low mosaic. This result was confirmed by FISH using BAC probes specific for chromosome 7. The SRC was a neocentric ring derived from 7q22.1q31.1 and was found in only 8% of the cells. This is the first patient carrying a mosaic neocentric SRC derived from the long arm of chromosome 7. Our study emphasizes the need to combine different techniques and to use adapted bioinformatic tools for low-mosaicism marker identification. It also contributes to the delineation of the partial trisomy 7q phenotype. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:111 / 117
页数:7
相关论文
共 50 条
  • [1] Prenatal diagnosis of a de novo small supernumerary ring chromosome 7
    Lebbar, A.
    Tantau, I.
    Cuisset, L.
    Le Du, N.
    Letessier, D.
    Rabineau, D.
    Dupont, J. M.
    [J]. CHROMOSOME RESEARCH, 2005, 13 : 135 - 135
  • [2] Molecular Cytogenetic Characterization of a de novo Mosaic Supernumerary Ring Chromosome 7: Report of a New Patient
    Bertini, Veronica
    Valetto, Angelo
    Uccelli, Angela
    Bonuccelli, Alice
    Tarantino, Enrico
    Taddeucci, Grazia
    Simi, Paolo
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2008, 146A (22) : 2955 - 2959
  • [3] Prenatal diagnosis of a de novo supernumerary marker derived from chromosome 16
    Hengstschläger, M
    Bettelheim, D
    Drahonsky, R
    Deutinger, J
    Bernaschek, G
    [J]. PRENATAL DIAGNOSIS, 2001, 21 (06) : 477 - 480
  • [4] First report of a supernumerary neocentric chromosome 6
    Sala, E.
    Crosti, F.
    Villa, N.
    Oldrini, A.
    Lalatta, F.
    Gandolfi, P.
    Gautiero, E.
    Solanol, R.
    Dalpra, L.
    [J]. CHROMOSOME RESEARCH, 2005, 13 : 131 - 132
  • [5] True fetal mosaicism for a supernumerary de novo ring chromosome.
    Meck, JM
    Wray, A
    Ghidini, A
    Gorman, B
    Vallejo, P
    Dennis, T
    Haddad, B
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 306 - 306
  • [6] Characterization of a small supernumerary ring marker derived from chromosome 2 by forward and reverse chromosome painting
    Ostroverkhova, NV
    Nazarenko, SA
    Rubtsov, NB
    Nazarenko, LP
    Bunina, EN
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1999, 87 (03): : 217 - 220
  • [7] PRENATAL DIAGNOSIS OF A DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATING FROM CHROMOSOME 16
    Yakut, S.
    Cetin, Z.
    Simsek, M.
    Karauzum, S. B.
    Tukun, A.
    Luleci, G.
    [J]. GENETIC COUNSELING, 2009, 20 (04): : 327 - 332
  • [8] Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male
    Sofia Kitsiou-Tzeli
    Emmanouil Manolakos
    Magdalini Lagou
    Maria Kontodiou
    Nadezda Kosyakova
    Elisabeth Ewers
    Anja Weise
    Antonios Garas
    Sandro Orru
    Thomas Liehr
    Aikaterini Metaxotou
    [J]. Molecular Cytogenetics, 2
  • [9] Characterization of a Mosaic de novo Small Supernumerary Ring Chromosome 2: Genotype-Phenotype Correlation
    Oliveira, Fernanda Paula
    Ribeiro, Joana
    Freitas, Manuela Mota
    Teles, Natalia Oliva
    Bartolo, Amelia
    Fonseca e Silva, Maria da Luz
    [J]. CHROMOSOME RESEARCH, 2013, 21 : S63 - S64
  • [10] Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male
    Kitsiou-Tzeli, Sofia
    Manolakos, Emmanouil
    Lagou, Magdalini
    Kontodiou, Maria
    Kosyakova, Nadezda
    Ewers, Elisabeth
    Weise, Anja
    Garas, Antonios
    Orru, Sandro
    Liehr, Thomas
    Metaxotou, Aikaterini
    [J]. MOLECULAR CYTOGENETICS, 2009, 2