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Alagille Syndrome: An ultrafiltration dilemma
Author(s) -
Catarina Abrantes,
Teresa Furtado,
Patrícia Domingues,
Patrícia Valério,
Joana Felgueiras,
José Assunção,
Álvaro Vaz
Publication year - 2021
Publication title -
revista portuguesa de nefrologia e hipertensão
Language(s) - English
Resource type - Journals
eISSN - 2183-1289
pISSN - 0872-0169
DOI - 10.32932/pjnh.2021.10.148
Subject(s) - medicine , alagille syndrome , ultrafiltration (renal) , biology , biochemistry , cholestasis
Alagille syndrome (AGLS) is a rare genetic disorder caused by mutations in the Notch signaling pathway. Multiple organ dysfunction is frequent despite phenotypic variability. We report the case of an AGLS patient with right heart failure and persistent fluid overload who started peritoneal ultrafiltration, without initial benefit. Possible pathophysiological mechanisms related to the underlying genetic condition, namely vascular abnormalities, that could help explain the poor ultrafiltration are provided, while other ultrafiltration failure causes are briefly discussed. New evidence is necessary for a better understanding of this syndrome in PD modality.

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