Factors Associated With the Development and Severity of Polycystic Liver in Patients With Autosomal Dominant Polycystic Kidney Disease
CONCLUSION: Hepatic involvement in ADPKD could be related to kidney manifestations and genetic variants including PKD1-PT or PKD2. Monitoring hemoglobin and ALP and evaluating the genetic variants might help predict severe PLD.TRIAL REGISTRATION: Clinical Research Information Service Identifier: KCT0005580.PMID:37750370 | PMC:PMC10519778 | DOI:10.3346/jkms.2023.38.e296
Source: J Korean Med Sci - Category: General Medicine Authors: Yaerim Kim Hayne Cho Park Hyunjin Ryu Yong Chul Kim Curie Ahn Kyu-Beck Lee Yeong Hoon Kim Seungyeup Han Eun Hui Bae Kyungjo Jeong Jungmin Choi Kook-Hwan Oh Yun Kyu Oh Source Type: research
More News: Epidemiology | General Medicine | Genetics | Laboratory Medicine | Liver | Liver Disease | Polycystic Kidney Disease | Study | Urology & Nephrology