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dc.contributor.authorFarrugia, Marie Claire-
dc.contributor.authorCalleja-Agius, Jean-
dc.date.accessioned2020-07-14T08:30:51Z-
dc.date.available2020-07-14T08:30:51Z-
dc.date.issued2016-
dc.identifier.citationFarrugia, M. C., & Calleja-Agius, J. (2016). Polydactyly : a review. Neonatal Network, 35(3), 135-142.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar/handle/123456789/58695-
dc.description.abstractPolydactyly, also known as hyperdactyly, is a common congenital limb defect, which can present with various morphologic phenotypes. Apart from cosmetic and functional impairments, it can be the first indication of an underlying syndrome in the newborn. Usually, it follows an autosomal dominant pattern of inheritance with defects occurring in the anteroposterior patterning of limb development. Although many mutations have been discovered, teratogens have also been implicated in leading to this anomaly, thus making it of multifactorial origin. There are three polydactyly subtypes (radial, ulnar, and central), and treatment options depend on the underlying feature.en_GB
dc.language.isoenen_GB
dc.publisherSpringer Publishing Companyen_GB
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_GB
dc.subjectExtremities (Anatomy) -- Abnormalitiesen_GB
dc.subjectAbnormalities, Humanen_GB
dc.subjectExtremities (Anatomy) -- Surgeryen_GB
dc.titlePolydactyly : a reviewen_GB
dc.typearticleen_GB
dc.rights.holderThe copyright of this work belongs to the author(s)/publisher. The rights of this work are as defined by the appropriate Copyright Legislation or as modified by any successive legislation. Users may access this work and can make use of the information contained in accordance with the Copyright Legislation provided that the author must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the prior permission of the copyright holder.en_GB
dc.description.reviewedpeer-revieweden_GB
dc.identifier.doi10.1891/0730-0832.35.3.135-
dc.publication.titleNeonatal Networken_GB
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