{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,27]],"date-time":"2026-10-27T19:56:22Z","timestamp":1793130982242,"version":"4.5.0"},"reference-count":25,"publisher":"Mathematical Modelling and Numerical Simulation with Applications","issue":"01","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Pediatr Genet"],"published-print":{"date-parts":[[2024,3]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Chromatinopathy is an emerging category of multiple malformation syndromes caused by disruption in global transcriptional regulation with imbalances in the chromatin states (i.e., open or closed chromatin). These syndromes are caused by pathogenic variants in genes coding for the writers, erasers, readers, and remodelers of the epigenetic machinery. Majority of these disorders (93%) show neurological dysfunction in the form of intellectual disability. Other overlapping features are growth abnormalities, limb deformities, and immune dysfunction. In this study, we describe a series of children with six common chromatinopathy syndromes with an aim to develop pattern recognition of this emerging category of multiple malformation syndromes<\/jats:p>","DOI":"10.1055\/s-0042-1748019","type":"journal-article","created":{"date-parts":[[2022,6,27]],"date-time":"2022-06-27T19:21:20Z","timestamp":1656357680000},"page":"006-014","source":"Crossref","is-referenced-by-count":4,"title":["Pattern Recognition of Common Multiple Congenital Malformation Syndromes with Underlying Chromatinopathy"],"prefix":"10.53391","volume":"13","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-5307-5677","authenticated-orcid":false,"given":"Anupriya","family":"Kaur","sequence":"additional","affiliation":[{"name":"Department of Paediatrics, Genetic Metabolic Unit, Post Graduate Institute of Medical Education and Research, Chandigarh, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0080-2172","authenticated-orcid":false,"given":"Chakshu","family":"Chaudhry","sequence":"additional","affiliation":[{"name":"Department of Paediatrics, Genetic Metabolic Unit, Post Graduate Institute of Medical Education and Research, Chandigarh, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3817-7122","authenticated-orcid":false,"given":"Parminder","family":"Kaur","sequence":"additional","affiliation":[{"name":"Department of Paediatrics, Genetic Metabolic Unit, Post Graduate Institute of Medical Education and Research, Chandigarh, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Roshan","family":"Daniel","sequence":"additional","affiliation":[{"name":"Department of Paediatrics, Genetic Metabolic Unit, Post Graduate Institute of Medical Education and Research, Chandigarh, 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