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A Critical Evaluation of the Down Syndrome Diagnosis for LB1, Type Specimen of Homo floresiensis

dc.contributor.authorBaab, Karen L
dc.contributor.authorBrown, Peter
dc.contributor.authorFalk, Dean
dc.contributor.authorRichtsmeier, Joan T
dc.contributor.authorHildebolt, Charles F
dc.contributor.authorSmith, Kirk
dc.contributor.authorJungers, William
dc.date.accessioned2016-08-19T01:55:44Z
dc.date.available2016-08-19T01:55:44Z
dc.date.issued2016
dc.description.abstractThe Liang Bua hominins from Flores, Indonesia, have been the subject of intense scrutiny and debate since their initial description and classification in 2004. These remains have been assigned to a new species, Homo floresiensis, with the partial skeleton LB1 as the type specimen. The Liang Bua hominins are notable for their short stature, small endocranial volume, and many features that appear phylogenetically primitive relative to modern humans, despite their late Pleistocene age. Recently, some workers suggested that the remains represent members of a small-bodied island population of modern Austro-Melanesian humans, with LB1 exhibiting clinical signs of Down syndrome. Many classic Down syndrome signs are soft tissue features that could not be assessed in skeletal remains. Moreover, a definitive diagnosis of Down syndrome can only be made by genetic analysis as the phenotypes associated with Down syndrome are variable. Most features that contribute to the Down syndrome phenotype are not restricted to Down syndrome but are seen in other chromosomal disorders and in the general population. Nevertheless, we re-evaluated the presence of those phenotypic features used to support this classification by comparing LB1 to samples of modern humans diagnosed with Down syndrome and euploid modern humans using comparative morphometric analyses. We present new data regarding neurocranial, brain, and symphyseal shape in Down syndrome, additional estimates of stature for LB1, and analyses of inter- and intralimb proportions. The presence of cranial sinuses is addressed using CT images of LB1. We found minimal congruence between the LB1 phenotype and clinical descriptions of Down syndrome. We present important differences between the phenotypes of LB1 and individuals with Down syndrome, and quantitative data that characterize LB1 as an outlier compared with Down syndrome and non-Down syndrome groups. Homo floresiensis remains a phenotypically unique, valid species with its roots in Plio-Pleistocene Homo taxa.en_AU
dc.description.sponsorshipGrant support was provided to KLB by the National Science Foundation (BCS 04-24262; http:// www.nsf.gov/), the L.S.B. Leakey Foundation (http:// www.leakeyfoundation.org/), and the Sigma Xi Foundation (https://www.sigmaxi.org/). JTR was supported in part by a National Institutes of Health grant (R01-HD038384; http://www.nih.gov/)en_AU
dc.identifier.issn1932-6203en_AU
dc.identifier.urihttp://hdl.handle.net/1885/107241
dc.publisherPublic Library of Scienceen_AU
dc.rights© 2016 Baab et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_AU
dc.sourcePloS oneen_AU
dc.titleA Critical Evaluation of the Down Syndrome Diagnosis for LB1, Type Specimen of Homo floresiensisen_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.issue6en_AU
local.bibliographicCitation.startpagee0155731en_AU
local.contributor.affiliationBrown, P., School of Archaeology & Anthropology, The Australian National Universityen_AU
local.contributor.authoruidu9112501en_AU
local.identifier.citationvolume11en_AU
local.identifier.doi10.1371/journal.pone.0155731en_AU
local.identifier.essn1932-6203en_AU
local.publisher.urlhttps://www.plos.org/en_AU
local.type.statusPublished Versionen_AU

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