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Congenital bilateral absence of vas deferens in the absence of cystic fibrosis

✍ Scribed by A. Augarten; Y. Yahav; J. Laufer; A. Szeinberg; J. Dor; S. Mashiach; I. Madgar; D. Halle; E. Gazit; B.S. Kerem

Book ID: 118554239
Publisher: The Lancet
Year: 1994
Tongue: English
Weight: 336 KB
Volume: 344
Category: Article
ISSN: 0140-6736
DOI: 10.1016/s0140-6736(94)90292-5

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CF and CBAVD are really just ends of a clinical spectrum. The type and nature of the mutations in the CF gene probably determine the phenotypic expression of the patient. Perhaps all patients homozygous for AF508, for example, will have severe pulmonary and pancreatic disease as well as absent vasa,