Literature DB >> 17668239

An unexpected finding in a child with neurological problems: mosaic ring chromosome 18.

Altuğ Koç1, Derya Kan, Kadri Karaer, Mehmet A Ergün, Meral Yirmibeş Karaoğuz, Kivilcim Gücüyener, Sophie Hinreiner, Thomas Liehr, E Ferda Perçin.   

Abstract

Major neurological disorders may accompany rare chromosomal abnormalities. As an example of this rare condition, we present a case with microcephaly, mental retardation, developmental delay, hyperactivity, stereotypic movements, seizures and dysmorphic facial appearance in whom a mosaic ring chromosome 18 was found [45,XX,-18/46,XX,r(18)/46,XX,dicr(18)]. Although ring chromosome 18 phenotype has been known for a long time, this is the third reported patient with a dicentric ring chromosome 18 mosaicism. The presented case will contribute to the identification of the genotype-phenotype correlation in chromosome 18 anomalies.

Entities:  

Mesh:

Year:  2007        PMID: 17668239     DOI: 10.1007/s00431-007-0568-y

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  21 in total

1.  Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18.

Authors:  P Stankiewicz; I Brozek; Z Hélias-Rodzewicz; J Wierzba; J Pilch; E Bocian; A Balcerska; A Wozniak; I Kardaś; J Wirth; T Mazurczak; J Limon
Journal:  Am J Med Genet       Date:  2001-07-01

2.  Transmission of ring chromosome 18 46,XX/46,XX,r(18) mosaicism in a mother and ring chromosome 18 syndrome in her son.

Authors:  J P Fryns; A Kleczkowska; E Smeets; H Van Den Berghe
Journal:  Ann Genet       Date:  1992

3.  18q deletions: clinical, molecular, and brain MRI findings of 14 individuals.

Authors:  Tarja Linnankivi; Pentti Tienari; Mirja Somer; Marketta Kähkönen; Tuula Lönnqvist; Leena Valanne; Helena Pihko
Journal:  Am J Med Genet A       Date:  2006-02-15       Impact factor: 2.802

4.  Transmission of a ring chromosome 18 from a mother with 46,XX/47,XX, + r(18) mosaicism to her daughter, resulting in a 46,XX,r(18) karyotype.

Authors:  J Jenderny; A Caliebe; C Beyer; W Grote
Journal:  J Med Genet       Date:  1993-11       Impact factor: 6.318

5.  Agammaglobulinaemia in a girl with a mosaic of ring 18 chromosome.

Authors:  J Litzman; V Brysová; R Gaillyová; V Thon; A Pijácková; K Michalová; Z Zemanová; J Lokaj
Journal:  J Paediatr Child Health       Date:  1998-02       Impact factor: 1.954

6.  Insulin dependent diabetes mellitus (IDDM) and autoimmune thyroiditis in a boy with a ring chromosome 18: additional evidence of autoimmunity or IDDM gene(s) on chromosome 18.

Authors:  C Dacou-Voutetakis; A Sertedaki; M Maniatis-Christidis; C Sarri; G Karadima; M B Petersen; A Xaidara; M Kanariou; P Nicolaidou
Journal:  J Med Genet       Date:  1999-02       Impact factor: 6.318

7.  Clinical and molecular characterization of individuals with 18p deletion: a genotype-phenotype correlation.

Authors:  Ulrika Wester; Marie-Louise Bondeson; Christina Edeby; Göran Annerén
Journal:  Am J Med Genet A       Date:  2006-06-01       Impact factor: 2.802

8.  Chromosome studies in IgA-deficient patients.

Authors:  R D Taalman; C M Weemaes; T W Hustinx; J M Scheres; J M Clement; G B Stoelinga
Journal:  Clin Genet       Date:  1987-08       Impact factor: 4.438

9.  Hypothalamic growth hormone deficiency in a patient with ring chromosome 18.

Authors:  A Meloni; L Boccone; L Angius; S Loche; A M Falchi; A Cao
Journal:  Eur J Pediatr       Date:  1994-02       Impact factor: 3.183

10.  Epileptic seizures, arthrogryposis, and migrational brain disorders: a syndrome?

Authors:  E Brodtkorb; T Torbergsen; K O Nakken; K Andersen; R Gimse; O Sjaastad
Journal:  Acta Neurol Scand       Date:  1994-10       Impact factor: 3.209

View more
  6 in total

1.  Ring chromosome 18: a case report.

Authors:  Shermineh Heydari; Fahimeh Hassanzadeh; Mohammad Hassanzadeh Nazarabadi
Journal:  Int J Mol Cell Med       Date:  2014

Review 2.  Ring chromosomes: from formation to clinical potential.

Authors:  Inna E Pristyazhnyuk; Aleksei G Menzorov
Journal:  Protoplasma       Date:  2017-09-12       Impact factor: 3.356

3.  Somatic mosaicism in cases with small supernumerary marker chromosomes.

Authors:  Thomas Liehr; Tatyana Karamysheva; Martina Merkas; Lukrecija Brecevic; Ahmed B Hamid; Elisabeth Ewers; Kristin Mrasek; Nadezda Kosyakova; Anja Weise
Journal:  Curr Genomics       Date:  2010-09       Impact factor: 2.236

4.  Molecular characterization and evaluation of complex rearrangements in a case of ring chromosome 15.

Authors:  Stuti Tewari; Naznin Lubna; Raju Shah; Ahmed B H Al-Rikabi; Krati Shah; Jayesh Sheth; Frenny Sheth
Journal:  Mol Cytogenet       Date:  2017-10-25       Impact factor: 2.009

5.  Chromosome abnormalities in Indonesian patients with short stature.

Authors:  Chrysantine Paramayuda; Hannie Kartapradja; Debby D Ambarwati; Helena W Anggaratri; Lita P Suciati; Nanis S Marzuki; Alida Harahap
Journal:  Mol Cytogenet       Date:  2012-08-06       Impact factor: 2.009

6.  Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patients.

Authors:  Haoran Ji; Dongxiao Li; Ye Wu; Quanli Zhang; Qiang Gu; Han Xie; Taoyun Ji; Huifang Wang; Lu Zhao; Haijuan Zhao; Yanling Yang; Hongchun Feng; Hui Xiong; Jinhua Ji; Zhixian Yang; Liping Kou; Ming Li; Xinhua Bao; Xingzhi Chang; Yuehua Zhang; Li Li; Huijuan Li; Zhengping Niu; Xiru Wu; Jiangxi Xiao; Yuwu Jiang; Jingmin Wang
Journal:  PLoS One       Date:  2018-02-16       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.