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Combined liver-kidney transplant for the management of methylmalonic aciduria: a case report and review of the literature Mc Guire PJ; Lim-Melia E; Diaz GA; Raymond K; Larkin A; Wasserstein MP; Sansaricq CMol Genet Metab 2008[Jan]; 93 (1): 22-9Over 27 cases of liver transplant, kidney transplant and combined liver-kidney transplant have been reported for the treatment of methylmalonic aciduria. We describe a case of a 5-year-old boy who underwent combined liver-kidney transplant (CLKT) for phenotypic mut0 disease. His history was notable for more than 30 hospitalizations for severe acidosis, metabolic strokes, liver disease, pancreatic disease, chronic renal insufficiency with interstitial nephritis, and decreased quality of life. Post-CLKT, there was a marked reduction in serum (80%) and urine MMA levels (90%) as well as a cessation of metabolic decompensations. Neurologic deterioration continued post-CKLT manifested as a cerebellar stroke. The clinical details and therapeutic implications of solid organ transplant for methylmalonic aciduria are discussed.|*Kidney Transplantation[MESH]|*Liver Transplantation/rehabilitation[MESH]|*Methylmalonic Acid/urine[MESH]|Amino Acid Metabolism, Inborn Errors/complications/*therapy[MESH]|Child, Preschool[MESH]|Developmental Disabilities/etiology[MESH]|Humans[MESH]|Lipid Metabolism, Inborn Errors/complications/*therapy[MESH]|Male[MESH] |
