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pubmed-article:10955475pubmed:dateCreated2000-11-27lld:pubmed
pubmed-article:10955475pubmed:abstractTextSpondylometaphyseal dysplasia of the Sedaghatian type is a rare dysplasia, characterized by mild limb shortening, but lethal in the neonatal period. We describe three affected male siblings, the offspring of consanguineous parents. One was stillborn. Neonatal death was due to cardiac arrhythmia in two of the siblings. This report confirms the importance of cardiac pathology in this probably autosomal recessive disorder. This diagnosis should be excluded in any newborn with an arrhythmia as the clinical limb shortening may not be obvious.lld:pubmed
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pubmed-article:10955475pubmed:authorpubmed-author:SillenceD ODOlld:pubmed
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pubmed-article:10955475pubmed:pagination167-72lld:pubmed
pubmed-article:10955475pubmed:dateRevised2007-11-15lld:pubmed
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pubmed-article:10955475pubmed:articleTitleSpondylometaphyseal dysplasia Sedaghatian type associated with lethal arrhythmia and normal intrauterine growth in three siblings.lld:pubmed
pubmed-article:10955475pubmed:affiliationDepartment of Genetics, Royal Manchester Children's Hospital, UK.lld:pubmed
pubmed-article:10955475pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10955475pubmed:publicationTypeCase Reportslld:pubmed