Combined kidney and liver transplantation for familial haemolytic uraemic syndrome.
Saved in:
| Title: | Combined kidney and liver transplantation for familial haemolytic uraemic syndrome. |
|---|---|
| Authors: | Remuzzi, Giuseppe, Ruggenenti, Piero, Codazzi, Daniela, Noris, Marina, Caprioli, Jessica, Locatelli, Giuseppe, Gridelli, Bruno |
| Source: | Lancet. 5/11/2002, Vol. 359 Issue 9318, p1671. 2p. 1 Diagram. |
| Subjects: | Hemolytic-uremic syndrome, Acute kidney failure, Kidney transplantation, Liver transplantation |
| Abstract: | Recurrent haemolytic uraemic syndrome (HUS) is a genetic form of thrombotic microangiopathy that is mostly associated with low activity of complement factor H. The disorder usually develops in families, leads to end stage renal disease, and invariably recurs after kidney transplantation. We did a simultaneous kidney and liver transplantation in a 2-year-old child with HUS and a mutation in complement factor H to restore the defective factor H, with no recurrence of the disease. The operation was successful, and at discharge, the child had healthy kidney and liver function, with no sign of haemolysis. [ABSTRACT FROM AUTHOR] |
| Copyright of Lancet is the property of Lancet and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Psychology and Behavioral Sciences Collection |
|
Full text is not displayed to guests.
Login for full access.
|
|
| FullText | Links: – Type: pdflink Text: Availability: 1 |
|---|---|
| Header | DbId: pbh DbLabel: Psychology and Behavioral Sciences Collection An: 6637811 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Combined kidney and liver transplantation for familial haemolytic uraemic syndrome. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Remuzzi%2C+Giuseppe%22">Remuzzi, Giuseppe</searchLink><br /><searchLink fieldCode="AR" term="%22Ruggenenti%2C+Piero%22">Ruggenenti, Piero</searchLink><br /><searchLink fieldCode="AR" term="%22Codazzi%2C+Daniela%22">Codazzi, Daniela</searchLink><br /><searchLink fieldCode="AR" term="%22Noris%2C+Marina%22">Noris, Marina</searchLink><br /><searchLink fieldCode="AR" term="%22Caprioli%2C+Jessica%22">Caprioli, Jessica</searchLink><br /><searchLink fieldCode="AR" term="%22Locatelli%2C+Giuseppe%22">Locatelli, Giuseppe</searchLink><br /><searchLink fieldCode="AR" term="%22Gridelli%2C+Bruno%22">Gridelli, Bruno</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Lancet%22">Lancet</searchLink>. 5/11/2002, Vol. 359 Issue 9318, p1671. 2p. 1 Diagram. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Hemolytic-uremic+syndrome%22">Hemolytic-uremic syndrome</searchLink><br /><searchLink fieldCode="DE" term="%22Acute+kidney+failure%22">Acute kidney failure</searchLink><br /><searchLink fieldCode="DE" term="%22Kidney+transplantation%22">Kidney transplantation</searchLink><br /><searchLink fieldCode="DE" term="%22Liver+transplantation%22">Liver transplantation</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Recurrent haemolytic uraemic syndrome (HUS) is a genetic form of thrombotic microangiopathy that is mostly associated with low activity of complement factor H. The disorder usually develops in families, leads to end stage renal disease, and invariably recurs after kidney transplantation. We did a simultaneous kidney and liver transplantation in a 2-year-old child with HUS and a mutation in complement factor H to restore the defective factor H, with no recurrence of the disease. The operation was successful, and at discharge, the child had healthy kidney and liver function, with no sign of haemolysis. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Lancet is the property of Lancet and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=pbh&AN=6637811 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/S0140-6736(02)08560-4 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 2 StartPage: 1671 Subjects: – SubjectFull: Hemolytic-uremic syndrome Type: general – SubjectFull: Acute kidney failure Type: general – SubjectFull: Kidney transplantation Type: general – SubjectFull: Liver transplantation Type: general Titles: – TitleFull: Combined kidney and liver transplantation for familial haemolytic uraemic syndrome. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Remuzzi, Giuseppe – PersonEntity: Name: NameFull: Ruggenenti, Piero – PersonEntity: Name: NameFull: Codazzi, Daniela – PersonEntity: Name: NameFull: Noris, Marina – PersonEntity: Name: NameFull: Caprioli, Jessica – PersonEntity: Name: NameFull: Locatelli, Giuseppe – PersonEntity: Name: NameFull: Gridelli, Bruno IsPartOfRelationships: – BibEntity: Dates: – D: 11 M: 05 Text: 5/11/2002 Type: published Y: 2002 Identifiers: – Type: issn-print Value: 01406736 Numbering: – Type: volume Value: 359 – Type: issue Value: 9318 Titles: – TitleFull: Lancet Type: main |
| ResultId | 1 |