causing amyloid angiopathy and brain hemorrhage ‐ clinical genetics in Iceland

• Published in: Clinical Genetics
• Main Authors: Jensson, Olafur, Palsdottir, Astridur, Thorsteinsson, Leifur, Arnason, Alfred
• Format: Article in Journal/Newspaper
• Language: English
• Published: Wiley 1989
• Subjects: Iceland
• Online Access: http://dx.doi.org/10.1111/j.1399-0004.1989.tb03215.x; https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1399-0004.1989.tb03215.x; https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1399-0004.1989.tb03215.x

Firstly, we review investigations of hereditary cystatin C amyloid angiopathy, which is caused by a mutation in the cystatin C gene. Symptoms of brain haemorrhages, which lead to death in young adults, are the hallmark of this disorder. The mutation can now be detected by the RFLP method using Alu I restriction enzyme and cystatin C cDNA probe. Secondly, we give an overview of other clinical genetic studies in Iceland with emphasis on activities initiated or sponsored by the Genetical Committee of the University of Iceland. The list of references covers most publications on genetic studies of Icelanders.