| Literature DB >> 33955014 |
Ilaria Parenti1, Mark B Mallozzi2, Irina Hüning3, Cristina Gervasini4, Alma Kuechler1, Emanuele Agolini5, Beate Albrecht1, Carolina Baquero-Montoya6,7, Axel Bohring8, Nuria C Bramswig1, Andreas Busche8, Andreas Dalski3, Yiran Guo9, Britta Hanker3, Yorck Hellenbroich3, Denise Horn10, A Micheil Innes11, Chiara Leoni12, Yun R Li9,13, Sally Ann Lynch14, Milena Mariani15, Livija Medne16,17, Barbara Mikat1, Donatella Milani18, Roberta Onesimo12, Xilma Ortiz-Gonzalez19,20, Eva Christina Prott1,21, Heiko Reutter22,23, Eva Rossier24,25, Angelo Selicorni15, Peter Wieacker8, Alisha Wilkens16, Dagmar Wieczorek26, Elaine H Zackai16,17, Giuseppe Zampino12, Birgit Zirn25, Hakon Hakonarson9,17, Matthew A Deardorff27,28, Gabriele Gillessen-Kaesbach3, Frank J Kaiser1,29.
Abstract
Mutations affecting the transcriptional regulator Ankyrin Repeat Domain 11 (ANKRD11) are mainly associated with the multisystem developmental disorder known as KBG syndrome, but have also been identified in individuals with Cornelia de Lange syndrome (CdLS) and other developmental disorders caused by variants affecting different chromatin regulators. The extensive functional overlap of these proteins results in shared phenotypical features, which complicate the assessment of the clinical diagnosis. Additionally, re-evaluation of individuals at a later age occasionally reveals that the initial phenotype has evolved toward clinical features more reminiscent of a developmental disorder different from the one that was initially diagnosed. For this reason, variants in ANKRD11 can be ascribed to a broader class of disorders that fall within the category of the so-called chromatinopathies. In this work, we report on the clinical characterization of 23 individuals with variants in ANKRD11. The subjects present primarily with developmental delay, intellectual disability and dysmorphic features, and all but two received an initial clinical diagnosis of either KBG syndrome or CdLS. The number and the severity of the clinical signs are overlapping but variable and result in a broad spectrum of phenotypes, which could be partially accounted for by the presence of additional molecular diagnoses and distinct pathogenic mechanisms.Entities:
Keywords: ANKRD11; Cornelia de Lange syndrome (CdLS); KBG syndrome (KBGS); chromatinopathies; developmental disorders
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Year: 2021 PMID: 33955014 DOI: 10.1111/cge.13977
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438