Zobrazeno 1 - 10
of 918
pro vyhledávání: '"Autoimmune Polyglandular Syndrome"'
Publikováno v:
Pediatria Polska, Vol 99, Iss 1, Pp 84-88 (2024)
Autoimmune polyglandular syndrome type 2 (APS-2) is the coexistence of Addison disease and at least one of the disorders like autoimmune thyroid diseases and/or type 1 diabetes mellitus. We discuss the case of 16.5-year-old girl who had been diagnose
Externí odkaz:
https://doaj.org/article/0e5fbcd210264d719fa7da25e902552d
Publikováno v:
Journal of Mazandaran University of Medical Sciences, Vol 33, Iss 227, Pp 345-349 (2023)
Schmidt syndrome is a polyendocrinopathy characterized by multiple organ failures. Patients with two or more of the following characteristics are diagnosed with this syndrome: Graves' disease, adrenal insufficiency, autoimmune thyroiditis, and type I
Externí odkaz:
https://doaj.org/article/19b85efdeed54befbadf540328dc6905
Autor:
Marta Arrigoni, Paolo Cavarzere, Lara Nicolussi Principe, Rossella Gaudino, Franco Antoniazzi
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-6 (2023)
Abstract Background Primary adrenal insufficiency (PAI) in childhood is a life-threatening disease most commonly due to impaired steroidogenesis. Differently from adulthood, autoimmune adrenalitis is a rare condition amongst PAI’s main aetiologies
Externí odkaz:
https://doaj.org/article/79e35ada31084c258c8063d220d22382
Publikováno v:
South African Medical Journal, Vol 114, Iss 1 (2023)
A 45-year-old female presented with unprovoked recurrent venous thromboembolism (VTE), in unusual sites, and pancytopenia, posing a complex diagnostic challenge. Work-up for inherited thrombophilia, antiphospholipid syndrome (APLS) and paroxysmal noc
Externí odkaz:
https://doaj.org/article/067e3c26fd8d460fa6f035e55d40e213
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 73, Iss 6 (2023)
Autoimmune polyglandular syndromes (APS) are rare disorders involving multiple endocrine and non-endocrine organs. These are often difficult to diagnose, as the clinical presentation of these is insidious. We present a case where a 29-year-old man pr
Externí odkaz:
https://doaj.org/article/1c1166b8d49d489fb20034e761787ada
Autor:
Elisa Gatta, Valentina Anelli, Elena Cimino, Elena Di Lodovico, Elda Piovani, Irene Zammarchi, Giorgia Gozzoli, Virginia Maltese, Maria Cavadini, Barbara Agosti, Andrea Delbarba, Ilenia Pirola, Angela Girelli, Caterina Buoso, Francesca Bambini, Daniele Alfieri, Walter Bremi, Paolo Facondo, Roberto Lupo, Francesco Bezzi, Micaela Fredi, Anna Maria Mazzola, Elena Gandossi, Maura Saullo, Fiorella Marini, Massimo Licini, Letizia Chiara Pezzaioli, Laura Pini, Franco Franceschini, Chiara Ricci, Carlo Cappelli
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
PurposeTo characterize patients with APS type 4 among those affected by APS diagnosed and monitored at our local Reference Center for Autoimmune Polyglandular Syndromes.MethodsMonocentric observational retrospective study enrolling patients affected
Externí odkaz:
https://doaj.org/article/905752b25ea0468d81abcffa23ae643f
Autor:
CONCEPCIÓN CARRILLO LE, RODRÍGUEZ PIÑA MD, PINEDA GONZÁLEZ MG, GARCÍA OCAMPO F, MENDIETA ZERÓN H
Publikováno v:
Паёми Сино, Vol 24, Iss 4, Pp 562-568 (2022)
Objective: Autoimmune polyglandular syndromes (APS) are endocrinopathies whose main characteristic is the loss of immune tolerance. The objective of this work was to report the APS prevalence in an Internal Medicine Service from Toluca, Mexico. Me
Externí odkaz:
https://doaj.org/article/d2b488a50735481d8e09fe2d462b3d29
Publikováno v:
Case Reports in Clinical Practice, Vol 8, Iss 1 (2023)
To this day, millions of people in the world have been diagnosed with corona virus 2019 (COVID-19). This disease cannot only lead to higher mortality rates among those with underlying Diabetes Mellitus (DM), but also may trigger DM in susceptible pat
Externí odkaz:
https://doaj.org/article/cb3ca9c09bdb4442b3a115665309dc33
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Медицинский вестник Юга России, Vol 13, Iss 2, Pp 168-171 (2022)
Type 1 autoimmune polyglandular syndrome (APS1) is a rare disease, with an unknown prevalence in the Russian population. Due to the low awareness of doctors, it takes more time to make the accurate diagnosis and provide correct medical care. This art
Externí odkaz:
https://doaj.org/article/1010187138f346cda5d92b4c0bd38b4e