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pubmed-article:8323498pubmed:abstractTextA case of microcephalic, osteodysplastic, primordial dwarfism (cephaloskeletal dysplasia of Taybi and Linder) is reported. This rare disease is characterised by unique clinical appearances and diagnostic radiographic findings. It is also associated with distinctive brain abnormalities. The latter include micrencephaly, lissencephaly, corpus callosum aplasia/agenesis and unusual histological brain abnormalities.lld:pubmed
pubmed-article:8323498pubmed:languageenglld:pubmed
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pubmed-article:8323498pubmed:authorpubmed-author:WrightR GRGlld:pubmed
pubmed-article:8323498pubmed:authorpubmed-author:KozlowskiKKlld:pubmed
pubmed-article:8323498pubmed:authorpubmed-author:MaselJJlld:pubmed
pubmed-article:8323498pubmed:authorpubmed-author:DonovanTTlld:pubmed
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pubmed-article:8323498pubmed:volume37lld:pubmed
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pubmed-article:8323498pubmed:pagination111-4lld:pubmed
pubmed-article:8323498pubmed:dateRevised2009-11-11lld:pubmed
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pubmed-article:8323498pubmed:year1993lld:pubmed
pubmed-article:8323498pubmed:articleTitleMicrocephalic, osteodysplastic, primordial dwarfism.lld:pubmed
pubmed-article:8323498pubmed:affiliationDepartment of Radiology, Royal Alexandra Hospital for Children, Sydney, Australia.lld:pubmed
pubmed-article:8323498pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8323498pubmed:publicationTypeCase Reportslld:pubmed
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