Anti-GPIHBP1 Antibody-Positive Autoimmune Hyperchylomicronemia and Immune Thrombocytopenia

Primary hyperchylomicronemia is characterized by marked hypertriglyceridemia exceeding 1,000 mg/dL. It is caused by dysfunctional mutations in specific genes, namely those for lipoprotein lipase (LPL), glycosylphosphatidylinositol-anchored high-density lipoprotein binding protein 1 (GPIHBP1), apolip...

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Detalles Bibliográficos
Autores principales: Tanaka, Katsunao, Koseki, Masahiro, Kato, Hisashi, Miyashita, Kazuya, Okada, Takeshi, Kanno, Kotaro, Saga, Ayami, Chang, Jiuyang, Omatsu, Takashi, Inui, Hiroyasu, Ohama, Tohru, Nishida, Makoto, Yamashita, Shizuya, Sakata, Yasushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japan Atherosclerosis Society 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9899696/
https://www.ncbi.nlm.nih.gov/pubmed/35185060
http://dx.doi.org/10.5551/jat.63348

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9899696/
https://www.ncbi.nlm.nih.gov/pubmed/35185060
http://dx.doi.org/10.5551/jat.63348

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