Kurzrippenpolydaktyliesyndrom vom Typ Verma-Naumoff

Abstract
A human infant male with perinatal lethal dwarfism is described due to its clinical, radiological and histologic features the case can be classified as SRP [short rib-polydactyly] syndrome type III (Verma-Naumoff). Based on radiological features and, particularly, on those of the growing cartilage, stress is laid on the importance of these studies for a proper classification of such rare and not completely known chondrodysplastic dwarfisms.

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