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Published in 2020 at "Scandinavian Journal of Urology"
DOI: 10.1080/21681805.2020.1798505
Abstract: The patient was a 68-year-old female with a confirmed genetic diagnosis of HHT (mutation in the ACVRL1 gene) with a strong family history of the disease. She had typical manifestations of telangiec...
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Keywords:
renal pelvis;
intractable bleeding;
patient hereditary;
bleeding renal ... See more keywords