Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients

The SOGRI Consortium, Jair Tenorio, Pablo Alarcón, Pedro Arias, Irene Dapía, Sixto García-Miñaur, María Palomares Bralo, Jaume Campistol, Salvador Climent, Irene Valenzuela, Sergio Ramos, Antonio Martínez Monseny, Fermina López Grondona, Javier Botet, Mercedes Serrano, Mario Solís, Fernando Santos-Simarro, Sara Álvarez, Gisela Teixidó-Tura, Alberto Fernández Jaén & 31 others Gema Gordo, María Belén Bardón Rivera, Julián Nevado, Alicia Hernández, Juan C. Cigudosa, Víctor L. Ruiz-Pérez, Eduardo F. Tizzano, Alberto L. Rosa, Aleixandre Blanquer, Alfredo García Alix, Alfredo Santana, Alicia Delicado, Almudena Alonso, Amaya Rodríguez, Amparo Sanchis, Ana Moreno, Ana Patiño García, Ana Vega, Analía Bredani, Andrea Paula Solari, Andrea Villavicencio, Angelina Acosta, Aníbal Nieto, Anna María Cueto González, Antonio Baldellon, Antonio González Meneses, Antonio Martínez Carrascal, Aranzazu Díaz de Bustamante, Arteche Ocasar, Blanca Gener, Luis Perez-Jurado

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Abstract

Tatton-Brown-Rahman (TBRS) syndrome is a recently described overgrowth syndrome caused by loss of function variants in the DNMT3A gene. This gene encodes for a DNA methyltransferase 3 alpha, which is involved in epigenetic regulation, especially during embryonic development. Somatic variants in DNMT3A have been widely studied in different types of tumors, including acute myeloid leukemia, hematopoietic, and lymphoid cancers. Germline gain-of-function variants in this gene have been recently implicated in microcephalic dwarfism. Common clinical features of patients with TBRS include tall stature, macrocephaly, intellectual disability (ID), and a distinctive facial appearance. Differential diagnosis of TBRS comprises Sotos, Weaver, and Malan Syndromes. The majority of these disorders present other clinical features with a high clinical overlap, making necessary a molecular confirmation of the clinical diagnosis. We here describe seven new patients with variants in DNMT3A, four of them with neuropsychiatric disorders, including schizophrenia and psychotic behavior. In addition, one of the patients has developed a brain tumor in adulthood. This patient has also cerebral atrophy, aggressive behavior, ID, and abnormal facial features. Clinical evaluation of this group of patients should include a complete neuropsychiatric assessment together with psychological support in order to detect and manage abnormal behaviors such as aggressiveness, impulsivity, and attention deficit-hyperactivity disorder. TBRS should be suspected in patients with overgrowth, ID, tall stature, and macrocephaly, who also have some neuropsychiatric disorders without any genetic defects in the commonest overgrowth disorders. Molecular confirmation in these patients is mandatory.

LanguageEnglish
Pages469-479
Number of pages11
JournalEuropean Journal of Human Genetics
Volume28
Issue number4
DOIs
Publication statusPublished - 1 Apr 2020

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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