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

被引:0
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作者
Mata, Marina [1 ,2 ,3 ]
Tabbara, Marina M. [1 ,2 ]
Alvarez, Angel [2 ]
Chandar, Jayanthi [4 ]
Defreitas, Marissa [4 ]
Ciancio, Gaetano [1 ,2 ,5 ]
机构
[1] Univ Miami, Miller Sch Med, Jackson Mem Hosp, Dept Surg, Miami, FL 33136 USA
[2] Univ Miami, Miller Sch Med, Jackson Mem Hosp, Miami Transplant Inst, Miami, FL 33136 USA
[3] Hosp Ramon & Cajal, Unidad Cirugia Renal Trasplante & Invest, Madrid, Spain
[4] Univ Miami, Miller Sch Med, Jackson Mem Hosp, Div Pediat Nephrol, Miami, FL 33136 USA
[5] Univ Miami, Miller Sch Med, Jackson Mem Hosp, Dept Surg & Urol, Miami, FL 33136 USA
关键词
Pediatric kidney transplantation; Oral-facial-digital syndrome type 1; Rare genetic disease; Case report; DIGITAL SYNDROME TYPE-1; RENAL-TRANSPLANTATION; COL4A1; MUTATIONS; INDUCTION THERAPY; CHILDREN; FAMILIES; OFD1;
D O I
10.1186/s12887-024-05304-x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BackgroundKidney 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 presentationWe 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.ConclusionsIn this case series, we discuss surgical technique, indication for kidney transplant, influence of comorbidities and intellectual disability in transplant outcomes.
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页数:8
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