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Oral Management of a Haematopoietic Stem Cell Transplant Recipient with Chédiak–Higashi Syndrome
Chédiak–Higashi syndrome (CHS), a rare autosomal recessive disorder associated with leukocyte dysfunction, is characterised by partial skin and hair albinism, immunodeficiency, and abnormal bleeding. Furthermore, it may be associated with cognitive and neurological impairments. The long-term prognos...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476280/ https://www.ncbi.nlm.nih.gov/pubmed/34589239 http://dx.doi.org/10.1155/2021/9918199 |
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author | Shimizu, Kasumi Hayashi, Miho Ito, Nozomi Hamada, Kokoro Koizumi, Gaku Kurohara, Kazuto Arai, Naoya |
author_facet | Shimizu, Kasumi Hayashi, Miho Ito, Nozomi Hamada, Kokoro Koizumi, Gaku Kurohara, Kazuto Arai, Naoya |
author_sort | Shimizu, Kasumi |
collection | PubMed |
description | Chédiak–Higashi syndrome (CHS), a rare autosomal recessive disorder associated with leukocyte dysfunction, is characterised by partial skin and hair albinism, immunodeficiency, and abnormal bleeding. Furthermore, it may be associated with cognitive and neurological impairments. The long-term prognosis of patients is generally poor, and haematopoietic stem cell transplantation is a radical immunodeficiency treatment. Here, we report a case of successful oral management of an 18-year-old woman with CHS accompanied by aggressive periodontitis who underwent haematopoietic stem cell transplantation. |
format | Online Article Text |
id | pubmed-8476280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-84762802021-09-28 Oral Management of a Haematopoietic Stem Cell Transplant Recipient with Chédiak–Higashi Syndrome Shimizu, Kasumi Hayashi, Miho Ito, Nozomi Hamada, Kokoro Koizumi, Gaku Kurohara, Kazuto Arai, Naoya Case Rep Dent Case Report Chédiak–Higashi syndrome (CHS), a rare autosomal recessive disorder associated with leukocyte dysfunction, is characterised by partial skin and hair albinism, immunodeficiency, and abnormal bleeding. Furthermore, it may be associated with cognitive and neurological impairments. The long-term prognosis of patients is generally poor, and haematopoietic stem cell transplantation is a radical immunodeficiency treatment. Here, we report a case of successful oral management of an 18-year-old woman with CHS accompanied by aggressive periodontitis who underwent haematopoietic stem cell transplantation. Hindawi 2021-09-20 /pmc/articles/PMC8476280/ /pubmed/34589239 http://dx.doi.org/10.1155/2021/9918199 Text en Copyright © 2021 Kasumi Shimizu et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Shimizu, Kasumi Hayashi, Miho Ito, Nozomi Hamada, Kokoro Koizumi, Gaku Kurohara, Kazuto Arai, Naoya Oral Management of a Haematopoietic Stem Cell Transplant Recipient with Chédiak–Higashi Syndrome |
title | Oral Management of a Haematopoietic Stem Cell Transplant Recipient with Chédiak–Higashi Syndrome |
title_full | Oral Management of a Haematopoietic Stem Cell Transplant Recipient with Chédiak–Higashi Syndrome |
title_fullStr | Oral Management of a Haematopoietic Stem Cell Transplant Recipient with Chédiak–Higashi Syndrome |
title_full_unstemmed | Oral Management of a Haematopoietic Stem Cell Transplant Recipient with Chédiak–Higashi Syndrome |
title_short | Oral Management of a Haematopoietic Stem Cell Transplant Recipient with Chédiak–Higashi Syndrome |
title_sort | oral management of a haematopoietic stem cell transplant recipient with chédiak–higashi syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476280/ https://www.ncbi.nlm.nih.gov/pubmed/34589239 http://dx.doi.org/10.1155/2021/9918199 |
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