Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study

Abstract The 22q11.2 deletion syndrome (22q11.2DS) is a multisystem disorder with an estimated prevalence of 1:3000 live births. Manifestations show a marked variability in expression and include speech‐ and language delay, intellectual disability, and neuropsychiatric disorders. We aim to provide an overview of ocular findings in 22q11.2DS in order to optimize recommendations for ophthalmic screening. We combined results from a systematic literature review with results from a multicenter cross‐sectional study of patients with 22q11.2DS who were assessed by an ophthalmologist. Our systematic l... Mehr ...

Verfasser: von Scheibler, Emma N. M. M.
van der Valk Bouman, Emy S.
Nuijts, Myrthe A.
Bauer, Noël J. C.
Berendschot, Tos T. J. M.
Vermeltfoort, Pit
Bok, Levinus A.
van Eeghen, Agnies M.
Houben, Michiel L.
van Amelsvoort, Thérèse A. M. J.
Boot, Erik
van Egmond‐Ebbeling, Michelle B.
Dokumenttyp: Artikel
Erscheinungsdatum: 2021
Reihe/Periodikum: American Journal of Medical Genetics Part A ; volume 188, issue 2, page 569-578 ; ISSN 1552-4825 1552-4833
Verlag/Hrsg.: Wiley
Schlagwörter: Genetics (clinical) / Genetics
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-27079657
Datenquelle: BASE; Originalkatalog
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Link(s) : http://dx.doi.org/10.1002/ajmg.a.62556