Literature DB >> 30108319

Familial total anomalous pulmonary venous return with 15q11.2 (BP1-BP2) microdeletion.

Yukiko Kuroda1, Ikuko Ohashi2, Takuya Naruto2, Kazumi Ida2, Yumi Enomoto2, Toshiyuki Saito3, Jun-Ichi Nagai3, Sadamitsu Yanagi4, Hideaki Ueda4, Kenji Kurosawa5.   

Abstract

A 15q11.2 microdeletion (BP1-BP2) is associated with congenital heart diseases (CHDs), developmental delay, and epilepsy. This deletion co-occurs with CHD in 20-30% patients, but a familial case of CHD and a 15q11.2 deletion has not been identified. Here we report the first familial (three siblings) case of total anomalous pulmonary venous return associated with 15q11.2 deletion. Array comparative genomic hybridization identified a ~395 kb deletion at 15q11.2 in patient 1. This deletion was confirmed by fluorescence in situ hybridization in patients 1 and 3 and their asymptomatic father. No deleterious mutation was identified by proband-only exome sequencing of patient 1. One healthy sibling and their mother did not carry the deletion. This deletion is often inherited from asymptomatic parents with an estimated low penetrance of 10.4%. Conversely, we observed high penetrance of this deletion, but secondary copy-number variants or pathogenic variants were not detected in this family.

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Year:  2018        PMID: 30108319     DOI: 10.1038/s10038-018-0499-7

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  16 in total

1.  Deletion of 15q11.2(BP1-BP2) region: further evidence for lack of phenotypic specificity in a pediatric population.

Authors:  Bita Hashemi; Anne Bassett; David Chitayat; Karen Chong; Mark Feldman; Janine Flanagan; Sharan Goobie; Anne Kawamura; Chelsea Lowther; Chitra Prasad; Victoria Siu; Joyce So; Sharon Tung; Marsha Speevak; Dimitri J Stavropoulos; Melissa T Carter
Journal:  Am J Med Genet A       Date:  2015-05-06       Impact factor: 2.802

2.  Change in prevalence of congenital defects in children with Prader-Willi syndrome.

Authors:  M Torrado; M E Foncuberta; M F de Castro Perez; L P Gravina; H V Araoz; E Baialardo; L P Chertkoff
Journal:  Pediatrics       Date:  2013-01-06       Impact factor: 7.124

3.  Transcriptional deregulation and a missense mutation define ANKRD1 as a candidate gene for total anomalous pulmonary venous return.

Authors:  Raffaella Cinquetti; Ileana Badi; Marina Campione; Elisabetta Bortoletto; Giulia Chiesa; Cinzia Parolini; Chiara Camesasca; Antonella Russo; Roberto Taramelli; Francesco Acquati
Journal:  Hum Mutat       Date:  2008-04       Impact factor: 4.878

4.  Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons.

Authors:  J-H Chai; D P Locke; J M Greally; J H M Knoll; T Ohta; J Dunai; A Yavor; E E Eichler; R D Nicholls
Journal:  Am J Hum Genet       Date:  2003-09-23       Impact factor: 11.025

5.  A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12.

Authors:  S Bleyl; L Nelson; S J Odelberg; H D Ruttenberg; B Otterud; M Leppert; K Ward
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

6.  Shared Segment Analysis and Next-Generation Sequencing Implicates the Retinoic Acid Signaling Pathway in Total Anomalous Pulmonary Venous Return (TAPVR).

Authors:  Dustin Nash; Cammon B Arrington; Brett J Kennedy; Mark Yandell; Wilfred Wu; Wenying Zhang; Stephanie Ware; Lynn B Jorde; Peter J Gruber; H Joseph Yost; Neil E Bowles; Steven B Bleyl
Journal:  PLoS One       Date:  2015-06-29       Impact factor: 3.240

7.  Total anomalous pulmonary venous return in siblings.

Authors:  Ho-Sung Kim; Kumi Jeong; Hwa-Jin Cho; Woo-Yeon Choi; Young Earl Choi; Jae Sook Ma; Young Kuk Cho
Journal:  J Cardiovasc Ultrasound       Date:  2014-12-26

8.  A novel UBE2A mutation causes X-linked intellectual disability type Nascimento.

Authors:  Yoshinori Tsurusaki; Ikuko Ohashi; Yumi Enomoto; Takuya Naruto; Jun Mitsui; Noriko Aida; Kenji Kurosawa
Journal:  Hum Genome Var       Date:  2017-06-08

9.  Whole-exome sequencing identifies SGCD and ACVRL1 mutations associated with total anomalous pulmonary venous return (TAPVR) in Chinese population.

Authors:  Jun Li; Shiwei Yang; Zhening Pu; Juncheng Dai; Tao Jiang; Fangzhi Du; Zhu Jiang; Yue Cheng; Genyin Dai; Jun Wang; Jirong Qi; Liming Cao; Xueying Cheng; Cong Ren; Xinli Li; Yuming Qin
Journal:  Oncotarget       Date:  2017-04-25

10.  Estimates of penetrance for recurrent pathogenic copy-number variations.

Authors:  Jill A Rosenfeld; Bradley P Coe; Evan E Eichler; Howard Cuckle; Lisa G Shaffer
Journal:  Genet Med       Date:  2012-12-20       Impact factor: 8.822

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  3 in total

1.  Recurrence pattern of non-syndromic familial congenital heart diseases among a large cohort of families from Egypt.

Authors:  Shaimaa Rakha; Rehab Mohy-Eldeen; Mohammad Al-Haggar; Mohammed Attia El-Bayoumi
Journal:  BMC Pediatr       Date:  2022-10-19       Impact factor: 2.567

2.  Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome.

Authors:  Kyle W Davis; Moises Serrano; Sara Loddo; Catherine Robinson; Viola Alesi; Bruno Dallapiccola; Antonio Novelli; Merlin G Butler
Journal:  Int J Mol Sci       Date:  2019-03-22       Impact factor: 5.923

3.  Total Anomalous Pulmonary Venous Connection in Mother and Son with a Central 22q11.2 Microdeletion.

Authors:  Signe Faurschou; Dorte L Lildballe; Lisa L Maroun; Morten Helvind; Maria Rasmussen
Journal:  Case Rep Genet       Date:  2021-06-10
  3 in total

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