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dc.contributor.authorPiranit N. Kantaputraen_US
dc.contributor.authorPranoot Tanpaiboonen_US
dc.date.accessioned2018-09-11T09:27:09Z-
dc.date.available2018-09-11T09:27:09Z-
dc.date.issued2005-01-01en_US
dc.identifier.issn15524825en_US
dc.identifier.other2-s2.0-11244304255en_US
dc.identifier.other10.1002/ajmg.a.30261en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=11244304255&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/62423-
dc.description.abstractWe report on a 3-year-old Thai boy with limb, pelvic, and genital malformations. The combination of findings found in this patient is similar to that of Al-Awadi/Raas-Rothchild syndrome (AARRS) or limb/pelvis hypoplasia/aplasia syndrome. The upper limbs are more severely affected than the lower ones. Unlike that of AARRS, the radial ray is more severely affected than the ulnar ray. The presence of humeroulnar synostosis and humero-ulnar-radial synostosis and the absence of a radius distinguishes it from AARRS. The similarities and dissimilarities between the features in the present patient and other limb-pelvic hypoplasia/aplasia syndromes are discussed. The findings in this group of patients appear to demonstrate limb-pelvis-genital organ developmental field defects. © 2004 Wiley-Liss, Inc.en_US
dc.subjectMedicineen_US
dc.titleA newly recognized syndrome involving limbs, pelvis, and genital organs or a variant of Al-Awadi/Raas-Rothschild syndrome?en_US
dc.typeJournalen_US
article.title.sourcetitleAmerican Journal of Medical Geneticsen_US
article.volume132 Aen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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