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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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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 |
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. |
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