Zobrazeno 1 - 10
of 1 261
pro vyhledávání: '"congenital hepatic fibrosis"'
Autor:
Savić Božidar, Milovanović Bojan, Stanojević Slobodan, Kureljušić Branislav, Jezdimirović Nemanja, Levakov Aleksandra Fejsa
Publikováno v:
Acta Veterinaria, Vol 74, Iss 2, Pp 313-321 (2024)
Congenital hepatic fibrosis (CHF) is a rare condition characterized by abnormal accumulation of fibrous tissue in the liver, leading to liver dysfunction. While CHF has been documented in various animal species, it has rarely been reported in cattle.
Externí odkaz:
https://doaj.org/article/5d15969a03e448fc973225753566ae07
Autor:
Jiawei Sun, Xiaoxiao Mi, Xiaoying Ye, Yiling ShenTu, Chun Liu, Dong Tang, WenJun Yang, Jie Yang, Xiaoping Ye, Xiaojie Ma, Junping Shi, Gongying Chen, Ling Gong
Publikováno v:
BMC Infectious Diseases, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Background CHF (Congenital hepatic fibrosis) is a rare hereditary disease characterized by periportal fibrosis and ductal plate malformation. Little is known about the clinical presentations and outcome in CHF patients with an extraordinary
Externí odkaz:
https://doaj.org/article/4e240690ef024639bbd158a6b8bdbb3c
Publikováno v:
Xin yixue, Vol 54, Iss 9, Pp 687-690 (2023)
Congenital hepatic fibrosis （CHF） complicated with Caroli’s disease is a rare autosomal recessive genetic disease with non-specific clinical and imaging manifestations， mainly including portal hypertension and complications， which is likely
Externí odkaz:
https://doaj.org/article/370b9c90d6274ab49e8706900aa78664
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
Congenital hepatic fibrosis (CHF) is considered to be a rare autosomal recessive hereditary fibrocystic liver disease, mainly found in children. However, cases of adult CHF with autosomal dominant polycystic kidney disease (ADPKD) caused by PKD1 gene
Externí odkaz:
https://doaj.org/article/32eeca11c0e246f3b52ecae6577a04b9
Akademický článek
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Autor:
Magd A. Kotb, Hend Abd El Baky, Shaimaa Sayed, Mohammed Al Komy, Marwa Onsy, Aya Aly, Andrew Tamer, Esraa Mohamed
Publikováno v:
Pediatric Sciences Journal, Vol 3, Iss 1, Pp 67-71 (2023)
Autosomal recessive polycystic kidney disease (ARPKD) is a rare genetic disorder that presents as an isolated polycystic renal disease in childhood, or associated with congenital hepatic fibrosis and/or Caroli disease. The spectrum of complications o
Externí odkaz:
https://doaj.org/article/7d4aaa361cc14993bb54e97bc4b3df2b
Publikováno v:
Balkan Journal of Medical Genetics, Vol 25, Iss 2, Pp 91-95 (2022)
Autosomal dominant polycystic kidney disease (ADKPD) is the most frequent type of polycystic kidney disease. It is inherited through family members, with an incidence of approximately 1:400 to1:1000.Typically, individuals with ADKPD are identified be
Externí odkaz:
https://doaj.org/article/dddaf1c950e8417e950524a9bc1d07d8
Publikováno v:
Asian Journal of Surgery, Vol 46, Iss 7, Pp 2888-2889 (2023)
Externí odkaz:
https://doaj.org/article/89ed6bb742f44b43964db532dc51263b
Publikováno v:
Zaporožskij Medicinskij Žurnal, Vol 23, Iss 6, Pp 882-888 (2021)
Congenital hepatic fibrosis (CHF) is an autosomal recessive disorder of intrauterine morphogenesis of the portobiliary system, characterized by periportal fibrosis and defective remodeling of the bile ducts. The article describes the features of the
Externí odkaz:
https://doaj.org/article/12ba9a77486040aa9288a9e246c40b4e
Akademický článek
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