An Anthropometric Study of 38 Individuals With Prader-Labhart- Willi Syndrome

dc.contributor.authorButler, Merlin G.
dc.contributor.authorMeaney, F. John
dc.contributor.authorOpitz, John M.
dc.contributor.authorReynolds, James F.
dc.contributor.departmentDepartment of Medical and Molecular Genetics, School of Medicineen_US
dc.date.accessioned2017-10-10T13:39:59Z
dc.date.available2017-10-10T13:39:59Z
dc.date.issued1987-02
dc.description.abstractWeight, height, sitting height, and 24 other anthropometric variables (5 body circumferences, skinfolds at 7 sites, 4 head dimensions, and 8 hand and foot measurements) were obtained on 38 Prader-Labhart-Willi syndrome (PLWS) individuals (21 with apparent chromosome 15 deletions and 17 nondeletion cases) with an age range of 2 weeks to 38½ years. More than half of these individuals were measured on more than one occasion. The measurements confirmed the presence of short stature, small hands and feet, obesity, and narrow bi-frontal diameter in PLWS. No differences were found for the anthropometric measurements between the 2 chromosome subgroups. Inverse correlations were produced with linear measurements (eg, height, hand and foot lengths) and age, which indicated a deceleration of linear growth relative to normal individuals with increasing age.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationButler, M. G., & Meaney, F. J. (1987). An Anthropometric Study of 38 Individuals With Prader-Labhart-Willi Syndrome. American Journal of Medical Genetics, 26(2), 445–455. http://doi.org/10.1002/ajmg.1320260224en_US
dc.identifier.urihttps://hdl.handle.net/1805/14279
dc.language.isoen_USen_US
dc.publisherWileyen_US
dc.relation.isversionof10.1002/ajmg.1320260224en_US
dc.relation.journalAmerican Journal of Medical Geneticsen_US
dc.rightsPublisher Policy
dc.sourcePMCen_US
dc.subjectChromosome 15 deletionen_US
dc.subjectCorrelation studiesen_US
dc.titleAn Anthropometric Study of 38 Individuals With Prader-Labhart- Willi Syndromeen_US
dc.typeArticleen_US
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