Articles with "stevenson syndrome" as a keyword



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Report of a Father With Congenital Bilateral Absence of the Vas Deferens Fathering a Child With Beare–Stevenson Syndrome

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Published in 2020 at "Frontiers in Genetics"

DOI: 10.3389/fgene.2020.00104

Abstract: Background Apert, Pfeiffer, and Crouzon syndromes are autosomal dominant diseases characterized by craniosynostosis. They are paternal age effect disorders. The association between paternal age and Beare–Stevenson syndrome (BSS), a very rare and severe craniosynostosis, is… read more here.

Keywords: beare stevenson; bilateral absence; age; congenital bilateral ... See more keywords