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ACTH therapy for West syndrome with severe hemophilia A
Hemophilia A is an X-linked recessive disorder caused by factor VIII deficiency, which is an important factor in the coagulation system. Here, we describe a 1-year-old boy with hemophilia A who developed West syndrome (WS). Recombinant factor VIII was administered during adrenocorticotropic hormone...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5118558/ https://www.ncbi.nlm.nih.gov/pubmed/27896066 http://dx.doi.org/10.1016/j.ebcr.2016.04.007 |
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author | Kubota, Kazuo Kinomura, Yoriko Yamamoto, Takahiro Ozeki, Michio Kawamoto, Minako Kawamoto, Norio Fukao, Toshiyuki |
author_facet | Kubota, Kazuo Kinomura, Yoriko Yamamoto, Takahiro Ozeki, Michio Kawamoto, Minako Kawamoto, Norio Fukao, Toshiyuki |
author_sort | Kubota, Kazuo |
collection | PubMed |
description | Hemophilia A is an X-linked recessive disorder caused by factor VIII deficiency, which is an important factor in the coagulation system. Here, we describe a 1-year-old boy with hemophilia A who developed West syndrome (WS). Recombinant factor VIII was administered during adrenocorticotropic hormone (ACTH) therapy to prevent intracranial hemorrhage. Infusion of factor VIII at fixed intervals is useful for the safe administration of ACTH therapy for patients with WS with severe hemophilia A. A coagulation screening test should be performed before ACTH therapy. |
format | Online Article Text |
id | pubmed-5118558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-51185582016-11-28 ACTH therapy for West syndrome with severe hemophilia A Kubota, Kazuo Kinomura, Yoriko Yamamoto, Takahiro Ozeki, Michio Kawamoto, Minako Kawamoto, Norio Fukao, Toshiyuki Epilepsy Behav Case Rep Case Report Hemophilia A is an X-linked recessive disorder caused by factor VIII deficiency, which is an important factor in the coagulation system. Here, we describe a 1-year-old boy with hemophilia A who developed West syndrome (WS). Recombinant factor VIII was administered during adrenocorticotropic hormone (ACTH) therapy to prevent intracranial hemorrhage. Infusion of factor VIII at fixed intervals is useful for the safe administration of ACTH therapy for patients with WS with severe hemophilia A. A coagulation screening test should be performed before ACTH therapy. Elsevier 2016-05-10 /pmc/articles/PMC5118558/ /pubmed/27896066 http://dx.doi.org/10.1016/j.ebcr.2016.04.007 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Kubota, Kazuo Kinomura, Yoriko Yamamoto, Takahiro Ozeki, Michio Kawamoto, Minako Kawamoto, Norio Fukao, Toshiyuki ACTH therapy for West syndrome with severe hemophilia A |
title | ACTH therapy for West syndrome with severe hemophilia A |
title_full | ACTH therapy for West syndrome with severe hemophilia A |
title_fullStr | ACTH therapy for West syndrome with severe hemophilia A |
title_full_unstemmed | ACTH therapy for West syndrome with severe hemophilia A |
title_short | ACTH therapy for West syndrome with severe hemophilia A |
title_sort | acth therapy for west syndrome with severe hemophilia a |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5118558/ https://www.ncbi.nlm.nih.gov/pubmed/27896066 http://dx.doi.org/10.1016/j.ebcr.2016.04.007 |
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