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Successful peritoneal dialysis for the end-stage kidney disease associated with Prader–Willi syndrome: a case report
Prader–Willi Syndrome (PWS) is characterized by hyperphagia, severe obesity, and mental retardation from early childhood and occurs 1/10,000 to 1/15,000 live births in Japan. There is high prevalence of diabetes mellitus because of hyperphagia. The patient may sometimes face the necessity of renal r...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620230/ https://www.ncbi.nlm.nih.gov/pubmed/30963414 http://dx.doi.org/10.1007/s13730-019-00395-3 |
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author | Anno, Emi Hori, Keiichiro Hoshimoto, Ainori Harano, Makiko Hagiwara, Sou Oishi, Kaori Yokoyama, Yoshinari Tsukamoto, Yusuke Kubota, Minoru |
author_facet | Anno, Emi Hori, Keiichiro Hoshimoto, Ainori Harano, Makiko Hagiwara, Sou Oishi, Kaori Yokoyama, Yoshinari Tsukamoto, Yusuke Kubota, Minoru |
author_sort | Anno, Emi |
collection | PubMed |
description | Prader–Willi Syndrome (PWS) is characterized by hyperphagia, severe obesity, and mental retardation from early childhood and occurs 1/10,000 to 1/15,000 live births in Japan. There is high prevalence of diabetes mellitus because of hyperphagia. The patient may sometimes face the necessity of renal replacement therapy (RRT) because of end-stage kidney disease (ESKD) caused by diabetes-associated kidney disease (DKD). Since mental retardation and extreme obesity usually prevent to introduce peritoneal dialysis (PD), hemodialysis (HD) has been the first choice of RRT. In this report, we experienced one case of patient with PWS suffering from ESKD due to DKD who started PD as an initial RRT and succeeded to continue for total of 40 months. The patient was 37-year-old man at the time of initiation of dialysis. PD was chosen for RRT because we suspected that he might have more technical difficulties for continuing HD. After several episodes of peritonitis, he successfully continues PD without peritonitis for next 27 months until the present time with good support by his family member. To our best knowledge, this is the first reported case of ESKD associated with PWS who was successfully treated with PD for long period. |
format | Online Article Text |
id | pubmed-6620230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-66202302019-07-28 Successful peritoneal dialysis for the end-stage kidney disease associated with Prader–Willi syndrome: a case report Anno, Emi Hori, Keiichiro Hoshimoto, Ainori Harano, Makiko Hagiwara, Sou Oishi, Kaori Yokoyama, Yoshinari Tsukamoto, Yusuke Kubota, Minoru CEN Case Rep Case Report Prader–Willi Syndrome (PWS) is characterized by hyperphagia, severe obesity, and mental retardation from early childhood and occurs 1/10,000 to 1/15,000 live births in Japan. There is high prevalence of diabetes mellitus because of hyperphagia. The patient may sometimes face the necessity of renal replacement therapy (RRT) because of end-stage kidney disease (ESKD) caused by diabetes-associated kidney disease (DKD). Since mental retardation and extreme obesity usually prevent to introduce peritoneal dialysis (PD), hemodialysis (HD) has been the first choice of RRT. In this report, we experienced one case of patient with PWS suffering from ESKD due to DKD who started PD as an initial RRT and succeeded to continue for total of 40 months. The patient was 37-year-old man at the time of initiation of dialysis. PD was chosen for RRT because we suspected that he might have more technical difficulties for continuing HD. After several episodes of peritonitis, he successfully continues PD without peritonitis for next 27 months until the present time with good support by his family member. To our best knowledge, this is the first reported case of ESKD associated with PWS who was successfully treated with PD for long period. Springer Singapore 2019-04-08 /pmc/articles/PMC6620230/ /pubmed/30963414 http://dx.doi.org/10.1007/s13730-019-00395-3 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Case Report Anno, Emi Hori, Keiichiro Hoshimoto, Ainori Harano, Makiko Hagiwara, Sou Oishi, Kaori Yokoyama, Yoshinari Tsukamoto, Yusuke Kubota, Minoru Successful peritoneal dialysis for the end-stage kidney disease associated with Prader–Willi syndrome: a case report |
title | Successful peritoneal dialysis for the end-stage kidney disease associated with Prader–Willi syndrome: a case report |
title_full | Successful peritoneal dialysis for the end-stage kidney disease associated with Prader–Willi syndrome: a case report |
title_fullStr | Successful peritoneal dialysis for the end-stage kidney disease associated with Prader–Willi syndrome: a case report |
title_full_unstemmed | Successful peritoneal dialysis for the end-stage kidney disease associated with Prader–Willi syndrome: a case report |
title_short | Successful peritoneal dialysis for the end-stage kidney disease associated with Prader–Willi syndrome: a case report |
title_sort | successful peritoneal dialysis for the end-stage kidney disease associated with prader–willi syndrome: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620230/ https://www.ncbi.nlm.nih.gov/pubmed/30963414 http://dx.doi.org/10.1007/s13730-019-00395-3 |
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