Literature DB >> 20503338

Multiple malignant diseases in a patient with Rothmund-Thomson syndrome with RECQL4 mutations: Case report and literature review.

T Simon1, J Kohlhase, C Wilhelm, M Kochanek, B De Carolis, F Berthold.   

Abstract

RECQL4 mutations cause genetic instability and increase the risk of malignant disease. We report on a patient with compound heterozygosity for two novel RECQL4 mutations: mutation c.1919_1924delTCACAG, p.L640_A642delinsP in exon 12 of the RECQL4 gene and mutation c.1704+1G>A in intron 10 of the RECQL4 gene. He subsequently developed large cell anaplastic T cell lymphoma at the age of 9 years, diffuse large cell B lymphoma and osteosarcoma when he was 14 years old, and finally acute lymphatic leukemia when he was 21 years old. The most remarkable clinical features are young age, spontaneous remission of diffuse large cell lymphoma, and severe CNS and skin toxicity of cytotoxic treatment. (c) 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20503338     DOI: 10.1002/ajmg.a.33427

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


  21 in total

1.  Rothmund-Thomson Syndrome-like RECQL4 truncating mutations cause a haploinsufficient low bone mass phenotype in mice.

Authors:  Wilson Castillo-Tandazo; Ann E Frazier; Natalie A Sims; Monique F Smeets; Carl R Walkley
Journal:  Mol Cell Biol       Date:  2020-12-23       Impact factor: 4.272

2.  Gastrointestinal Malignancy Presenting with a Virchow's Node in a Patient with Rothmund-Thomson Syndrome.

Authors:  Kara Nadeau; Michele Brule
Journal:  Case Rep Genet       Date:  2018-10-25

3.  Rothmund-Thomson syndrome (RTS) with osteosarcoma due to RECQL4 mutation.

Authors:  Anas Salih; Susumu Inoue; Nkechi Onwuzurike
Journal:  BMJ Case Rep       Date:  2018-01-23

4.  Human RECQ Helicase Pathogenic Variants, Population Variation and "Missing" Diseases.

Authors:  Wenqing Fu; Alessio Ligabue; Kai J Rogers; Joshua M Akey; Raymond J Monnat
Journal:  Hum Mutat       Date:  2016-12-09       Impact factor: 4.878

Review 5.  More than just skin deep: faciocutaneous clues to genetic syndromes with malignancies.

Authors:  Zhu Shen; Jodi D Hoffman; Fei Hao; Eric Pier
Journal:  Oncologist       Date:  2012-06-15

6.  Report of Two Novel Mutations in Indian Patients with Rothmund-Thomson Syndrome.

Authors:  Sakshi Yadav; Seema Thakur; Juergen Kohlhase; Neetu Bhari; Madhulika Kabra; Neerja Gupta
Journal:  J Pediatr Genet       Date:  2019-04-09

Review 7.  Recommendations for Childhood Cancer Screening and Surveillance in DNA Repair Disorders.

Authors:  Michael F Walsh; Vivian Y Chang; Wendy K Kohlmann; Hamish S Scott; Christopher Cunniff; Franck Bourdeaut; Jan J Molenaar; Christopher C Porter; John T Sandlund; Sharon E Plon; Lisa L Wang; Sharon A Savage
Journal:  Clin Cancer Res       Date:  2017-06-01       Impact factor: 12.531

8.  The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis.

Authors:  Monique F Smeets; Elisabetta DeLuca; Meaghan Wall; Julie M Quach; Alistair M Chalk; Andrew J Deans; Jörg Heierhorst; Louise E Purton; David J Izon; Carl R Walkley
Journal:  J Clin Invest       Date:  2014-06-24       Impact factor: 14.808

9.  RECQ helicase RECQL4 participates in non-homologous end joining and interacts with the Ku complex.

Authors:  Raghavendra A Shamanna; Dharmendra Kumar Singh; Huiming Lu; Gladys Mirey; Guido Keijzers; Bernard Salles; Deborah L Croteau; Vilhelm A Bohr
Journal:  Carcinogenesis       Date:  2014-06-18       Impact factor: 4.944

10.  Novel physiological RECQL4 alternative transcript disclosed by molecular characterisation of Rothmund-Thomson Syndrome sibs with mild phenotype.

Authors:  Elisa Adele Colombo; Laura Fontana; Gaia Roversi; Gloria Negri; Daniele Castiglia; Mauro Paradisi; Giovanna Zambruno; Lidia Larizza
Journal:  Eur J Hum Genet       Date:  2014-02-12       Impact factor: 4.246

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