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Orthotopic Heart Transplantation in a Patient With Gitelman Syndrome and Dilated Cardiomyopathy

Gitelman syndrome (GS) is a rare hereditary tubulopathy affecting the distal tubule leading to significant electrolyte disturbances.(1) Although generally a benign condition, rare associations with arrhythmias and sudden cardiac death have been reported.(1) A paucity of literature exists associating...

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Detalles Bibliográficos
Autores principales: Solt, Shannon Alexandra, Hoffman, Timothy M., Sharma, Mahesh S., Westreich, Katherine D., Kihlstrom, Margaret, Schwartz, Stephanie P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844390/
https://www.ncbi.nlm.nih.gov/pubmed/32645769
http://dx.doi.org/10.1177/2150135120912227
Descripción
Sumario:Gitelman syndrome (GS) is a rare hereditary tubulopathy affecting the distal tubule leading to significant electrolyte disturbances.(1) Although generally a benign condition, rare associations with arrhythmias and sudden cardiac death have been reported.(1) A paucity of literature exists associating GS with cardiomyopathy. We present a child with dilated cardiomyopathy and GS who was successfully treated with orthotopic heart transplantation.