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Pernicious Anemia in an Adult with Trisomy 21
Pernicious anemia is an autoimmune disease caused by the malabsorption of vitamin B12. It usually appears in the elderly. People with trisomy 21 are susceptible to autoimmune diseases. This susceptibility is thought to be due to altered expression of the AIRE gene, which is located in the 21q22.3 re...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474957/ https://www.ncbi.nlm.nih.gov/pubmed/37663274 http://dx.doi.org/10.1155/2023/2747756 |
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author | Kamada, Kentaro Kawano, Osamu Yakuwa, Satoshi Wakasa, Kentaro Uetake, Kimiaki |
author_facet | Kamada, Kentaro Kawano, Osamu Yakuwa, Satoshi Wakasa, Kentaro Uetake, Kimiaki |
author_sort | Kamada, Kentaro |
collection | PubMed |
description | Pernicious anemia is an autoimmune disease caused by the malabsorption of vitamin B12. It usually appears in the elderly. People with trisomy 21 are susceptible to autoimmune diseases. This susceptibility is thought to be due to altered expression of the AIRE gene, which is located in the 21q22.3 region. Although pernicious anemia is not common in people with trisomy 21, AIRE is pointed out as a susceptibility gene of pernicious anemia in a genome-wide association study. Here, we report a man with trisomy 21, who suffered from the pernicious anemia. When he was in his 30 s, he visited our hospital because of diarrhea and poor oral intake. He showed thrombocytopenic purpura-like features, and was diagnosed as pernicious anemia. After supplementation of vitamin B12, he recovered from the illness. The reason for his early onset may be because of trisomy 21. Altered expression of AIRE might trigger the disease. |
format | Online Article Text |
id | pubmed-10474957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-104749572023-09-03 Pernicious Anemia in an Adult with Trisomy 21 Kamada, Kentaro Kawano, Osamu Yakuwa, Satoshi Wakasa, Kentaro Uetake, Kimiaki Case Reports Immunol Case Report Pernicious anemia is an autoimmune disease caused by the malabsorption of vitamin B12. It usually appears in the elderly. People with trisomy 21 are susceptible to autoimmune diseases. This susceptibility is thought to be due to altered expression of the AIRE gene, which is located in the 21q22.3 region. Although pernicious anemia is not common in people with trisomy 21, AIRE is pointed out as a susceptibility gene of pernicious anemia in a genome-wide association study. Here, we report a man with trisomy 21, who suffered from the pernicious anemia. When he was in his 30 s, he visited our hospital because of diarrhea and poor oral intake. He showed thrombocytopenic purpura-like features, and was diagnosed as pernicious anemia. After supplementation of vitamin B12, he recovered from the illness. The reason for his early onset may be because of trisomy 21. Altered expression of AIRE might trigger the disease. Hindawi 2023-08-26 /pmc/articles/PMC10474957/ /pubmed/37663274 http://dx.doi.org/10.1155/2023/2747756 Text en Copyright © 2023 Kentaro Kamada 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 Kamada, Kentaro Kawano, Osamu Yakuwa, Satoshi Wakasa, Kentaro Uetake, Kimiaki Pernicious Anemia in an Adult with Trisomy 21 |
title | Pernicious Anemia in an Adult with Trisomy 21 |
title_full | Pernicious Anemia in an Adult with Trisomy 21 |
title_fullStr | Pernicious Anemia in an Adult with Trisomy 21 |
title_full_unstemmed | Pernicious Anemia in an Adult with Trisomy 21 |
title_short | Pernicious Anemia in an Adult with Trisomy 21 |
title_sort | pernicious anemia in an adult with trisomy 21 |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474957/ https://www.ncbi.nlm.nih.gov/pubmed/37663274 http://dx.doi.org/10.1155/2023/2747756 |
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