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Robinow syndrome with parental consanguinity.

D Glaser·J Herbst·K Roggenkamp·W Tünte·W Lenz
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Abstract

We describe the clinical features of Robinow syndrome in the first child of a consanguineous Turkish couple. This observation supports the view that severe vertebral anomalies are a feature of the autosomal-recessive form of Robinow syndrome.

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Abnormalities, MultipleConsanguinityDwarfismFaceFemaleHumansInfant, NewbornSyndromeCase ReportsJournal Article

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BibTeXRIS

D Glaser, J Herbst, K Roggenkamp, W Tünte, W Lenz. 1989. Robinow syndrome with parental consanguinity.. https://doi.org/10.1007/bf00441525

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