Literature DB >> 28584646

A novel mutation of NFIX causes Sotos-like syndrome (Malan syndrome) complicated with thoracic aortic aneurysm and dissection.

Tsukasa Oshima1, Hironori Hara1, Norifumi Takeda1, Eriko Hasumi1, Yukiko Kuroda2, Go Taniguchi3, Ryo Inuzuka2, Kan Nawata4, Hiroyuki Morita1, Issei Komuro1.   

Abstract

Malan syndrome has recently been characterized to present Sotos-like phenotypes, such as intellectual disability and macrocephaly, with mutations in the NFIX gene. Herein, we report a 38-year-old patient with a novel single adenine insertion mutation in exon 2 of the NFIX gene (c.290_291insA). He developed early-onset thoracic aortic aneurysm and dissection, which was a rare complication but deserves particular attention in relatively long-lived patients with Sotos-like phenotypes.

Entities:  

Year:  2017        PMID: 28584646      PMCID: PMC5451486          DOI: 10.1038/hgv.2017.22

Source DB:  PubMed          Journal:  Hum Genome Var        ISSN: 2054-345X


  12 in total

1.  NSD1 mutations are the major cause of Sotos syndrome and occur in some cases of Weaver syndrome but are rare in other overgrowth phenotypes.

Authors:  Jenny Douglas; Sandra Hanks; I Karen Temple; Sally Davies; Alexandra Murray; Meena Upadhyaya; Susan Tomkins; Helen E Hughes; Trevor R P Cole; Nazneen Rahman
Journal:  Am J Hum Genet       Date:  2002-12-02       Impact factor: 11.025

2.  Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes.

Authors:  Seval Türkmen; Gabriele Gillessen-Kaesbach; Peter Meinecke; Beate Albrecht; Luitgard M Neumann; Volker Hesse; Sükrü Palanduz; Stefanie Balg; Frank Majewski; Sigrun Fuchs; Petra Zschieschang; Monika Greiwe; Kirsten Mennicke; Friedmar R Kreuz; Harald J Dehmel; Burkhard Rodeck; Jürgen Kunze; Sigrid Tinschert; Stefan Mundlos; Denise Horn
Journal:  Eur J Hum Genet       Date:  2003-11       Impact factor: 4.246

3.  Distinct effects of allelic NFIX mutations on nonsense-mediated mRNA decay engender either a Sotos-like or a Marshall-Smith syndrome.

Authors:  Valérie Malan; Diana Rajan; Sophie Thomas; Adam C Shaw; Hélène Louis Dit Picard; Valérie Layet; Marianne Till; Arie van Haeringen; Geert Mortier; Sheela Nampoothiri; Silvija Puseljić; Laurence Legeai-Mallet; Nigel P Carter; Michel Vekemans; Arnold Munnich; Raoul C Hennekam; Laurence Colleaux; Valérie Cormier-Daire
Journal:  Am J Hum Genet       Date:  2010-07-30       Impact factor: 11.025

4.  Apparent germline mosaicism for a novel 19p13.13 deletion disrupting NFIX and CACNA1A.

Authors:  Manjunath Nimmakayalu; V Kim Horton; Ben Darbro; Shivanand R Patil; Hamza Alsayouf; Kim Keppler-Noreuil; Oleg A Shchelochkov
Journal:  Am J Med Genet A       Date:  2013-03-13       Impact factor: 2.802

Review 5.  Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature.

Authors:  Merel Klaassens; Deborah Morrogh; Elisabeth M Rosser; Fatima Jaffer; Maaike Vreeburg; Levinus A Bok; Tim Segboer; Martine van Belzen; Ros M Quinlivan; Ajith Kumar; Jane A Hurst; Richard H Scott
Journal:  Eur J Hum Genet       Date:  2014-08-13       Impact factor: 4.246

6.  Nuclear factor I X deficiency causes brain malformation and severe skeletal defects.

Authors:  Katrin Driller; Axel Pagenstecher; Markus Uhl; Heymut Omran; Ansgar Berlis; Albert Gründer; Albrecht E Sippel
Journal:  Mol Cell Biol       Date:  2007-05       Impact factor: 4.272

7.  The transcription factor Nfix is essential for normal brain development.

Authors:  Christine E Campbell; Michael Piper; Céline Plachez; Yu-Ting Yeh; Joan S Baizer; Jason M Osinski; E David Litwack; Linda J Richards; Richard M Gronostajski
Journal:  BMC Dev Biol       Date:  2008-05-13       Impact factor: 1.978

8.  Nfix Regulates Temporal Progression of Muscle Regeneration through Modulation of Myostatin Expression.

Authors:  Giuliana Rossi; Stefania Antonini; Chiara Bonfanti; Stefania Monteverde; Chiara Vezzali; Shahragim Tajbakhsh; Giulio Cossu; Graziella Messina
Journal:  Cell Rep       Date:  2016-02-25       Impact factor: 9.423

9.  A deleterious MYH11 mutation causing familial thoracic aortic dissection.

Authors:  Norifumi Takeda; Hiroyuki Morita; Daishi Fujita; Ryo Inuzuka; Yuki Taniguchi; Kan Nawata; Issei Komuro
Journal:  Hum Genome Var       Date:  2015-08-06

10.  NSD1 analysis for Sotos syndrome: insights and perspectives from the clinical laboratory.

Authors:  Darrel J Waggoner; Gordana Raca; Katherine Welch; Melissa Dempsey; Ethan Anderes; Irina Ostrovnaya; Asem Alkhateeb; Junichi Kamimura; Naomichi Matsumoto; G Bradley Schaeffer; Christa Lese Martin; Soma Das
Journal:  Genet Med       Date:  2005-10       Impact factor: 8.822

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  7 in total

1.  Aortic root dilatation and dilated cardiomyopathy in an adult with Tatton-Brown-Rahman syndrome.

Authors:  Alana C Cecchi; Amier Haidar; Isabella Marin; Callie S Kwartler; Siddharth K Prakash; Dianna M Milewicz
Journal:  Am J Med Genet A       Date:  2021-10-13       Impact factor: 2.578

2.  NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly.

Authors:  Ina Schanze; Jens Bunt; Jonathan W C Lim; Denny Schanze; Ryan J Dean; Marielle Alders; Patricia Blanchet; Tania Attié-Bitach; Siren Berland; Steven Boogert; Sangamitra Boppudi; Caitlin J Bridges; Megan T Cho; William B Dobyns; Dian Donnai; Jessica Douglas; Dawn L Earl; Timothy J Edwards; Laurence Faivre; Brieana Fregeau; David Genevieve; Marion Gérard; Vincent Gatinois; Muriel Holder-Espinasse; Samuel F Huth; Kosuke Izumi; Bronwyn Kerr; Elodie Lacaze; Phillis Lakeman; Sonal Mahida; Ghayda M Mirzaa; Sian M Morgan; Catherine Nowak; Hilde Peeters; Florence Petit; Daniela T Pilz; Jacques Puechberty; Eyal Reinstein; Jean-Baptiste Rivière; Avni B Santani; Anouck Schneider; Elliott H Sherr; Constance Smith-Hicks; Ilse Wieland; Elaine Zackai; Xiaonan Zhao; Richard M Gronostajski; Martin Zenker; Linda J Richards
Journal:  Am J Hum Genet       Date:  2018-11-01       Impact factor: 11.025

3.  Further delineation of Malan syndrome.

Authors:  Manuela Priolo; Denny Schanze; Katrin Tatton-Brown; Paul A Mulder; Jair Tenorio; Kreepa Kooblall; Inés Hernández Acero; Fowzan S Alkuraya; Pedro Arias; Laura Bernardini; Emilia K Bijlsma; Trevor Cole; Christine Coubes; Irene Dapia; Sally Davies; Nataliya Di Donato; Nursel H Elcioglu; Jill A Fahrner; Alison Foster; Noelia García González; Ilka Huber; Maria Iascone; Ann-Sophie Kaiser; Arveen Kamath; Jan Liebelt; Sally Ann Lynch; Saskia M Maas; Corrado Mammì; Inge B Mathijssen; Shane McKee; Leonie A Menke; Ghayda M Mirzaa; Tara Montgomery; Dorothee Neubauer; Thomas E Neumann; Letizia Pintomalli; Maria Antonietta Pisanti; Astrid S Plomp; Sue Price; Claire Salter; Fernando Santos-Simarro; Pierre Sarda; Mabel Segovia; Charles Shaw-Smith; Sarah Smithson; Mohnish Suri; Rita Maria Valdez; Arie Van Haeringen; Johanna M Van Hagen; Marcela Zollino; Pablo Lapunzina; Rajesh V Thakker; Martin Zenker; Raoul C Hennekam
Journal:  Hum Mutat       Date:  2018-06-25       Impact factor: 4.878

4.  MiR-663a Stimulates Proliferation and Suppresses Early Apoptosis of Human Spermatogonial Stem Cells by Targeting NFIX and Regulating Cell Cycle.

Authors:  Fan Zhou; Qingqing Yuan; Wenhui Zhang; Minghui Niu; Hongyong Fu; Qianqian Qiu; Guoping Mao; Hong Wang; Liping Wen; Hongxiang Wang; Mujun Lu; Zheng Li; Zuping He
Journal:  Mol Ther Nucleic Acids       Date:  2018-07-04       Impact factor: 8.886

Review 5.  Malan syndrome in a patient with 19p13.2p13.12 deletion encompassing NFIX and CACNA1A genes: Case report and review of the literature.

Authors:  Fernanda T Bellucco; Claudia B de Mello; Vera A Meloni; Maria Isabel Melaragno
Journal:  Mol Genet Genomic Med       Date:  2019-10-01       Impact factor: 2.183

6.  Characterization of Cognitive, Language and Adaptive Profiles of Children and Adolescents with Malan Syndrome.

Authors:  Paolo Alfieri; Marina Macchiaiolo; Martina Collotta; Federica Alice Maria Montanaro; Cristina Caciolo; Francesca Cumbo; Paolo Galassi; Filippo Maria Panfili; Fabiana Cortellessa; Marcella Zollino; Maria Accadia; Marco Seri; Marco Tartaglia; Andrea Bartuli; Corrado Mammì; Stefano Vicari; Manuela Priolo
Journal:  J Clin Med       Date:  2022-07-14       Impact factor: 4.964

7.  A deep phenotyping experience: up to date in management and diagnosis of Malan syndrome in a single center surveillance report.

Authors:  Marina Macchiaiolo; Filippo M Panfili; Davide Vecchio; Michaela V Gonfiantini; Fabiana Cortellessa; Cristina Caciolo; Marcella Zollino; Maria Accadia; Marco Seri; Marcello Chinali; Corrado Mammì; Marco Tartaglia; Andrea Bartuli; Paolo Alfieri; Manuela Priolo
Journal:  Orphanet J Rare Dis       Date:  2022-06-18       Impact factor: 4.303

  7 in total

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