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Article

Genetic syndromes are prevalent in patients with comorbid neurodevelopmental disorders and catatonia.

American journal of medical genetics. Part A - 1 Nov 2023

Shillington Amelle, Zappia Katherine J, White Lori, Fosdick Cara, Erickson Craig A, Lamy Martine, Dominick Kelli C

Abstract excerpt

Catatonia occurs at high rates in idiopathic and syndromic neurodevelopmental disorders. At our institution's multidisciplinary catatonia clinic, clinical genetic testing (including microarray, fragile X PCR and methylation, autism/ID expanded panels, and exome sequencing) was commonly completed as part of clinical workup on patients with co-occurring neurodevelopmental disorders and catatonia (performed in 36/48...

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Identifiers

PMID: 37642312
DOI: 10.1002/ajmg.a.63379

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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