Etiological diagnosis in limb reduction defects and the number of affected limbs: A population‐based study in the Northern Netherlands

Abstract Limb reduction defects (LRDs) that affect multiple limbs are considered to be more often heritable, but only few studies have substantiated this. We aimed to investigate if an etiological diagnosis (genetic disorder or clinically recognizable disorder) is more likely to be made when multiple limbs are affected compared to when only one limb is affected. We used data from EUROCAT Northern Netherlands and included 391 fetuses and children with LRDs born in 1981–2017. Cases were classified as having a transverse, longitudinal (preaxial/postaxial/central/mixed), intercalary, or complex LR... Mehr ...

Verfasser: Bergman, Jorieke E. H.
Löhner, Katharina
van der Sluis, Corry K.
Rump, Patrick
de Walle, Hermien E. K.
Dokumenttyp: Artikel
Erscheinungsdatum: 2020
Reihe/Periodikum: American Journal of Medical Genetics Part A ; volume 182, issue 12, page 2909-2918 ; ISSN 1552-4825 1552-4833
Verlag/Hrsg.: Wiley
Schlagwörter: Genetics (clinical) / Genetics
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26850871
Datenquelle: BASE; Originalkatalog
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Link(s) : http://dx.doi.org/10.1002/ajmg.a.61875