Zobrazeno 1 - 10
of 1 055
pro vyhledávání: '"Autoimmune syndrome"'
Autor:
Carolina Fux-Otta, Raúl Reynoso, Peter Chedraui, Paula Estario, María E. Estario, Gabriel Iraci, Noelia Ramos, Mariana Di Carlo, Victoria Gamba, Adela Sembaj
Publikováno v:
Case Reports in Women's Health, Vol 43, Iss , Pp e00644- (2024)
Insulin autoimmune syndrome or Hirata's disease is a rare condition characterized by hypoglycemia associated with endogenous autoimmune hyperinsulinism. This report concerns the case of a 28-year-old Latin American woman with Graves' disease who deve
Externí odkaz:
https://doaj.org/article/f3d209cbc3f0404ab3763e907e86905a
Autor:
Jordan Teoli, Karim Chikh, Ryme Jouini-Bouhamri, Sybil Charriere, Nicole Fabien, Véronique Raverot
Publikováno v:
Heliyon, Vol 10, Iss 13, Pp e34009- (2024)
Background: Determining the cause of hypoglycemia partly relies on blood insulin and C-peptide assays. Although the pancreatic secretion of these peptides is equimolar, discrepancies in their concentrations may occur. Case presentation: We report the
Externí odkaz:
https://doaj.org/article/9d8c07736aae4dbeabdfe05ff4f20511
Publikováno v:
The Egyptian Journal of Internal Medicine, Vol 36, Iss 1, Pp 1-3 (2024)
Abstract Background Insulin autoimmune antibody syndrome is an uncommon cause of hypoglycemia in non-diabetic individuals. We report a case of alpha-lipoic acid-induced insulin autoimmune antibody syndrome. Case report A 40-year-old non-diabetic fema
Externí odkaz:
https://doaj.org/article/548e2ec386d946b792805d8bf7c9b107
Publikováno v:
Journal of Diabetes Investigation, Vol 15, Iss 3, Pp 275-281 (2024)
Abstract This report describes a patient who developed recurrent hypoglycemia episodes after 23 days of antiplatelet therapy with clopidogrel for left subclavian artery stent implantation. The patient suffered from palpitation, profuse sweating and w
Externí odkaz:
https://doaj.org/article/66aec4aa669841c18b79c657343aa66b
Autor:
Ali M. Alrufaidi, Mohammed Mosa Alnashery, Ageel Ahmad Alghanimi, Rash Elamin Ahmed Elmansor, Ramy Mohamed Ghazy
Publikováno v:
Clinical Case Reports, Vol 12, Iss 6, Pp n/a-n/a (2024)
Key Clinical Message Autoimmune polyglandular syndrome type 1 (APS‐1) is a rare disorder defined by the presence of at least two of the following conditions: chronic mucocutaneous candidiasis (CMC), chronic hypoparathyroidism, and Addison's syndrom
Externí odkaz:
https://doaj.org/article/899379c1c80041398c39e9de7546302f
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
We report here the case of a 50-year-old man who was first diagnosed with myelodysplastic syndrome with excess blasts-2 (MDS-EB-2) and underwent allogeneic hematopoietic stem cell transplantation (allo-HSCT) in 2019, resulting in complete remission.
Externí odkaz:
https://doaj.org/article/5fd291bcd41544e9b6a7016575cc0523
Akademický článek
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Autor:
Lili Zhao, Jinzhi He, Shandong Ye, Chao Chen, Jie Zhu, Chunchun Xiao, Tingni Wu, Zhicheng Liu
Publikováno v:
BMC Endocrine Disorders, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background Insulin autoimmune syndrome (IAS) is a rare cause of hypoglycemia characterized by high levels of blood insulin autoantibodies. It has been documented that drugs containing sulfhydryl groups may result in IAS. In this study, we pr
Externí odkaz:
https://doaj.org/article/6bfe3d9d4d2b4d8abc74e4f66a853726
Publikováno v:
Frontiers in Neurology, Vol 14 (2024)
IntroductionThe cases of MOG-AD (MOG antibody-associated disorder) and anti-NMDAR encephalitis overlapping syndrome (MNOS) are rare, especially among pediatric patients, and their clinical understanding is limited. This study aimed to investigate the
Externí odkaz:
https://doaj.org/article/61566c0d47be49298526df4c868e983e
Publikováno v:
Romanian Medical Journal, Vol 70, Iss 2, Pp 98-101 (2023)
Objectives. We present a very rare case of incomplete Graham-Little-Piccardi-Lassueur syndrome (GLPLS) overlap with Mixed Connective Tissue Disease (MCTD) versus Multiple Autoimmune Syndrome (MAS). Case Presentation. A 53- year-old female with a long
Externí odkaz:
https://doaj.org/article/83a495a4237248f2a749371019bff584