Literature DB >> 18384145

Two new cases of pure 1q terminal deletion presenting with brain malformations.

Yoko Hiraki1, Nobuhiko Okamoto, Tomoko Ida, Yusei Nakata, Masahiro Kamada, Yonehiro Kanemura, Mami Yamasaki, Hiroko Fujita, Gen Nishimura, Mitsuhiro Kato, Naoki Harada, Naomichi Matsumoto.   

Abstract

We describe two new cases of pure 1q terminal deletions. BAC FISH analysis precisely defined the size of deletions. The first is a girl with 10.3-Mb deletion showed typical features of 1q43 deletion as well as a simplified gyral pattern, which was rarely found in 1q43 deletion. The other boy also presented with most of 1q43 deletion features but several atypical symptoms were noted including hydrocephalus, adducted thumbs, and flexion restriction of proximal interphalangeal joints in left hand. A concomitant novel missense mutation in L1CAM was identified in addition to 11.5-Mb deletion. Reviewing all the cases of pure 1q terminal deletion in the literature suggests that it is a clinically recognizable syndrome. 2008 Wiley-Liss, Inc.

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Year:  2008        PMID: 18384145     DOI: 10.1002/ajmg.a.32275

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  6 in total

1.  Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pair.

Authors:  Dilek Aktas; Eda G Utine; Kristin Mrasek; Anja Weise; Ferdinand von Eggeling; Kalbiye Yalaz; Nicole Posorski; Nurten Akarsu; Mehmet Alikasifoglu; Thomas Liehr; Ergul Tuncbilek
Journal:  Mol Cytogenet       Date:  2010-05-28       Impact factor: 2.009

2.  Prenatal diagnosis of a terminal chromosome 1 (q42-q44) deletion: original case report and review of the literature.

Authors:  C Van Linthout; V Emonard; J S Gatot; X Capelle; F Kridelka; P Emonts; M C Segghaye
Journal:  Facts Views Vis Obgyn       Date:  2016-06-27

3.  Chromosome microarray analysis in the investigation of children with congenital heart disease.

Authors:  Xiao-Li Wu; Ru Li; Fang Fu; Min Pan; Jin Han; Xin Yang; Yong-Ling Zhang; Fa-Tao Li; Can Liao
Journal:  BMC Pediatr       Date:  2017-05-04       Impact factor: 2.125

4.  Opposite chromosome constitutions due to a familial translocation t(1;21)(q43;q22) in 2 cousins with development delay and congenital anomalies: A case report.

Authors:  Beata Aleksiūnienė; Rugilė Matulevičiūtė; Aušra Matulevičienė; Birutė Burnytė; Natalija Krasovskaja; Laima Ambrozaitytė; Violeta Mikštienė; Vaidas Dirsė; Algirdas Utkus; Vaidutis Kučinskas
Journal:  Medicine (Baltimore)       Date:  2017-04       Impact factor: 1.889

5.  Constitutional 763.3 Kb chromosome 1q43 duplication encompassing only CHRM3 gene identified by next generation sequencing (NGS) in a child with intellectual disability.

Authors:  Xiaofei Cheng; Qifang Yang; Jun Liu; Juan Ye; Huiying Xiao; Gaimei Zhang; Yuanyuan Pan; Xia Li; Ruifeng Hao; Yinfeng Li
Journal:  Mol Cytogenet       Date:  2019-04-17       Impact factor: 2.009

6.  A chromosome 1q44 deletion in a 4-month-old girl; The first report in Korea.

Authors:  Joo Hyun Cho; Eun Song Song; Hee Na Kim; Burm Seok Oh; Young Youn Choi
Journal:  Korean J Pediatr       Date:  2014-06-30
  6 in total

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