Literature DB >> 31066180

The first case report of medulloblastoma associated with Tatton-Brown-Rahman syndrome.

Kieron J Sweeney1,2, Carmine Mottolese2, Alexandre Belot3, Alexandru Szathmari2, Didier Frappaz4, Gaetan Lesca5, Audrey Putoux6,7, Federico Di Rocco2.   

Abstract

DNMT3A codes for a DNA methyl transferase enzyme that plays a central role embryogenesis. Somatic mutations in this gene have been associated with tumorigenesis and are associated with a number of cancers. The recently described Tatton-Brown-Rahman syndrome (TBRS) is due to heterozygous germline mutations in the DNMT3A gene. So far, only one case of hematological malignancy associated with TBRS have been reported. Here, we describe the first case presenting with TBRS and medulloblastoma. We also discuss the associations between mutations in DNMT3A found in TBRS, AML, and medulloblastoma.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  Tatton-Brown-Rahman syndrome; medulloblastoma; overgrowth intellectual disability

Mesh:

Substances:

Year:  2019        PMID: 31066180     DOI: 10.1002/ajmg.a.61180

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


  5 in total

1.  DNMT3A overgrowth syndrome is associated with the development of hematopoietic malignancies in children and young adults.

Authors:  Margaret A Ferris; Amanda M Smith; Sharon E Heath; Eric J Duncavage; Matthew Oberley; David Freyer; Robert Wynn; Sofia Douzgou; John M Maris; Anne F Reilly; Melinda D Wu; Florence Choo; Roel B Fiets; Saskia Koene; David H Spencer; Christopher A Miller; Marwan Shinawi; Timothy J Ley
Journal:  Blood       Date:  2022-01-20       Impact factor: 22.113

2.  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

Review 3.  [Tatton-Brown-Rahman syndrome associated with the DNMT3A gene: a case report and literature review].

Authors:  Min Chen; Si-Tao Li; Yao Cai; Xin Xiao; Cong-Cong Shi; Hu Hao
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2020-10

4.  Dnmt3a deficiency in the skin causes focal, canonical DNA hypomethylation and a cellular proliferation phenotype.

Authors:  David Y Chen; Ian M Ferguson; Krista A Braun; Leslie A Sutton; Nichole M Helton; Sai Mukund Ramakrishnan; Amanda M Smith; Christopher A Miller; Timothy J Ley
Journal:  Proc Natl Acad Sci U S A       Date:  2021-04-20       Impact factor: 11.205

5.  Functional and epigenetic phenotypes of humans and mice with DNMT3A Overgrowth Syndrome.

Authors:  Amanda M Smith; Taylor A LaValle; Marwan Shinawi; Sai M Ramakrishnan; Haley J Abel; Cheryl A Hill; Nicole M Kirkland; Michael P Rettig; Nichole M Helton; Sharon E Heath; Francesca Ferraro; David Y Chen; Sangeeta Adak; Clay F Semenkovich; Diana L Christian; Jenna R Martin; Harrison W Gabel; Christopher A Miller; Timothy J Ley
Journal:  Nat Commun       Date:  2021-07-27       Impact factor: 14.919

  5 in total

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