BMC Pediatrics (Dec 2024)

Case series of kidney transplantation in two pediatric recipients with rare genetic diseases and intellectual disability

  • Marina Mata,
  • Marina M. Tabbara,
  • Angel Alvarez,
  • Jayanthi Chandar,
  • Marissa Defreitas,
  • Gaetano Ciancio

DOI
https://doi.org/10.1186/s12887-024-05304-x
Journal volume & issue
Vol. 24, no. 1
pp. 1 – 8

Abstract

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Abstract Background Kidney transplantation is the gold standard treatment for end-stage kidney disease in children. Rare genetic systemic diseases associated with cystic kidney disease such as COL4A1-related disorder and oral facial digital syndrome type 1 could contribute to end-stage kidney disease in the pediatric population but there is scarce evidence in the literature regarding kidney transplant outcomes in these cases. Case presentation We report a case of a 5-year-old male with COL4A1-related disorder who received a living-related donor kidney transplant from his mother. To our knowledge this is the first reported kidney transplant in a pediatric recipient with COL4A1-related disorder. We also present a case of a 16-year-old female with oral facial digital syndrome type 1 who received a deceased donor kidney transplant. Conclusions In this case series, we discuss surgical technique, indication for kidney transplant, influence of comorbidities and intellectual disability in transplant outcomes.

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