CTLA-4 gene mutation and multiple sclerosis: A case report and literature review

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DC Field	Value	Language
dc.contributor.author	-Wei Lin, Ting	-
dc.contributor.author	-Chiao Hu, Ya	-
dc.contributor.author	-Hsu Yang, Yao	-
dc.contributor.author	-Hsiu Chien, Yin	-
dc.contributor.author	-Chung Lee, Ni	-
dc.contributor.author	-Hui Yu, Hsin	-
dc.date.accessioned	2024-12-18T07:10:39Z	-
dc.date.available	2024-12-18T07:10:39Z	-
dc.date.issued	2022-06-01	-
dc.identifier.issn	1684-1182	-
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/9249	-
dc.description.abstract	Abstract We reported a patient with autoimmunity (multiple sclerosis), immunodeficiency (hypogammaglobulinemia with severe infections), enteropathy (diarrhea with intestinal inflammation), splenomegaly, lymphadenopathy and lymphocytic infiltration of nonlymphoid organs (lung, gut and brain). The patient was found to have a heterozygous mutation in cytotoxic T lymphocyte antigen-4, and had excellent response to abatacept.	en_US
dc.language.iso	en	en_US
dc.publisher	Elsevier Taiwan LLC	en_US
dc.subject	Abatacept;	en_US
dc.subject	Cytotoxic T lymphocyte antigen-4;	en_US
dc.subject	Multiple sclerosis;	en_US
dc.subject	Primary immunodeficiency	en_US
dc.title	CTLA-4 gene mutation and multiple sclerosis: A case report and literature review	en_US
dc.type	Article	en_US
Appears in Collections:	VOL 55 NO 3 2022

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