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pubmed-article:11977180pubmed:abstractTextWe describe a 33-day-old boy who had short and thick tibiae, symmetrical oligosyndactyly of the hands, and distinctive face. The patient was considered as a case of Nievergelt syndrome, a rare form of mesomelic dysplasia. Besides the characteristic mesomelic limb anomalies of Nievergelt syndrome, this patient exhibited two additional features: agenesis of the cerebellar vermis and cataracts, both of which have not been previously reported.lld:pubmed
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pubmed-article:11977180pubmed:authorpubmed-author:TüysüzBeyhanBlld:pubmed
pubmed-article:11977180pubmed:authorpubmed-author:ZorerGaziGlld:pubmed
pubmed-article:11977180pubmed:authorpubmed-author:ZeybekCenapClld:pubmed
pubmed-article:11977180pubmed:authorpubmed-author:SipahiOzlemOlld:pubmed
pubmed-article:11977180pubmed:authorpubmed-author:UngürSavasSlld:pubmed
pubmed-article:11977180pubmed:copyrightInfoCopyright 2002 Wiley-Liss, Inc.lld:pubmed
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pubmed-article:11977180pubmed:pagination206-10lld:pubmed
pubmed-article:11977180pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:11977180pubmed:year2002lld:pubmed
pubmed-article:11977180pubmed:articleTitlePatient with the mesomelic dysplasia, Nievergelt syndrome, and cerebellovermian agenesis and cataracts.lld:pubmed
pubmed-article:11977180pubmed:affiliationDivision of Genetics and Teratology, Department of Pediatrics, University of Istanbul, Istanbul, Turkey. beyhantuysuz@yahoo.comlld:pubmed
pubmed-article:11977180pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11977180pubmed:publicationTypeCase Reportslld:pubmed