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FSGS is known to recur after kidney transplantation, frequently followed by graft loss. However, not all patients with FSGS suffer from recurrence after kidney transplantation, and genetic and secondary FSGS have a negligible risk of recurrence. Furthermore, many cases of recurrence achieve remission with the current management of recurrence (intensive plasmapheresis\/immunosuppression, including rituximab), and other promising agents are being evaluated. Therefore, a pathologic diagnosis of FSGS itself should not cause postponement of allograft kidney transplantation. For patients with a high risk of recurrence who presented with classical symptoms of NS, that is, severe edema, proteinuria, and hypoalbuminemia, close monitoring of proteinuria is necessary, followed by immediate, intensive treatment for recurrence.<\/jats:p>","DOI":"10.1155\/2016\/6832971","type":"journal-article","created":{"date-parts":[[2016,4,24]],"date-time":"2016-04-24T21:00:53Z","timestamp":1461531653000},"page":"1-7","source":"Crossref","is-referenced-by-count":22,"title":["Recurrence and Treatment after Renal Transplantation in Children with FSGS"],"prefix":"10.1155","volume":"2016","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8323-5320","authenticated-orcid":true,"given":"Hee Gyung","family":"Kang","sequence":"first","affiliation":[{"name":"Department of Pediatrics, Seoul National University Hospital, Seoul 03080, Republic of Korea"},{"name":"Research Coordination Center for Rare Diseases, Seoul National University Hospital, Seoul 03080, Republic of 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