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Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens

✍ Scribed by Viktoria Havasi; Steven M. Rowe; Peter N. Kolettis; Didem Dayangac; Ahmet Şahin; Ana Grangeia; Filipa Carvalho; Alberto Barros; Mario Sousa; Lluis Bassas; Teresa Casals; Eric J. Sorscher


Book ID
116476552
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
110 KB
Volume
94
Category
Article
ISSN
1556-5653

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📜 SIMILAR VOLUMES


Congenital bilateral absence of the vas
✍ R. D. Oates; J. A. Amos 📂 Article 📅 1993 🏛 Springer-Verlag 🌐 English ⚖ 798 KB

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,