Zobrazeno 1 - 10
of 213
pro vyhledávání: '"polyglandular autoimmune syndrome"'
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
Autor:
Haoyang Wang, MD, Karen Feghali, MD, Vybhav A. Jetty, MD, Artem Astsaturov, MD, Darren M. Evanchuk, MD, Uyen Lam, MD, Ann T. Sweeney, MD
Publikováno v:
AACE Clinical Case Reports, Vol 7, Iss 6, Pp 353-356 (2021)
Objective: To report the first case, to our knowledge, of intermittent pancytopenia and cardiac tamponade occurring together in association with Autoimmune Addison's Disease (AAD). Methods: A 21 year-old woman presented on three different occasions w
Externí odkaz:
https://doaj.org/article/9042d9b440364ebfb5204c3b2b53d682
Autor:
Seo‐Young Hwang, Ju‐Hyun An, Jeong‐Hwa Lee, Su‐Min Park, Hyung Kyu Chae, Kyung‐Bo Kim, Woo‐Jin Song, Hwa‐Young Youn
Publikováno v:
Veterinary Medicine and Science, Vol 7, Iss 6, Pp 2120-2123 (2021)
Abstract Background Autoimmune polyendocrine syndrome, also called polyglandular autoimmune syndrome, is a rare immune‐mediated disorder that involves various endocrine glands. Purpose To report autoimmune polyendocrine syndrome in a dog. Methods A
Externí odkaz:
https://doaj.org/article/18834aa147cb44a6b835549e16d76e2b
Autor:
Ameer Kakaje, Rama Awad
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 2350-2352 (2020)
Abstract We are reporting a case report of Behcet's disease with autoimmune dysfunction that affected the thyroid and adrenal glands and the patient also had sub‐clinical celiac disease. However, the correlation between Bechet's disease and autoimm
Externí odkaz:
https://doaj.org/article/e65917f6184247eda59773bbd8561a37
BclI polymorphism of the glucocorticoid receptor and adrenal crisis in primary adrenal insufficiency
Publikováno v:
Endocrine Connections, Vol 6, Iss 8, Pp 685-691 (2017)
Context: Patients with primary adrenal insufficiency (PAI) or congenital adrenal hyperplasia (CAH) are at a high risk of adrenal crisis (AC). Glucocorticoid sensitivity is at least partially genetically determined by polymorphisms of the glucocortico
Externí odkaz:
https://doaj.org/article/d100989ad0ff45639de208921c66c9dc
Autor:
Dominique Endres, Patrick Süß, Simon J. Maier, Evelyn Friedel, Kathrin Nickel, Christiane Ziegler, Bernd L. Fiebich, Franz X. Glocker, Friedrich Stock, Karl Egger, Thomas Lange, Michael Dacko, Nils Venhoff, Daniel Erny, Soroush Doostkam, Katalin Komlosi, Katharina Domschke, Ludger Tebartz van Elst
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Background: Mitochondrial diseases are caused by dysfunctions in mitochondrial metabolic pathways. MELAS syndrome is one of the most frequent mitochondrial disorders; it is characterized by encephalopathy, myopathy, lactic acidosis, and stroke-like e
Externí odkaz:
https://doaj.org/article/a6dc33df1ba44dea8fe2b22e2358cb81
Autor:
Matteo Chinello, Margherita Mauro, Gaetano Cantalupo, Rita Balter, Massimiliano De Bortoli, Virginia Vitale, Ada Zaccaron, Elisa Bonetti, Rossella Gaudino, Elena Fiorini, Simone Cesaro
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
The polyglandular autoimmune syndrome type I is a rare hereditary autosomal recessive disease. We describe a child with the classic triad of the disease and her sister with pure red cell aplasia and cerebellar hypoplasia. The latter received two haem
Externí odkaz:
https://doaj.org/article/74534a58c2b748a08db2b75c6c8d21ca
Autor:
Darren M. Evanchuk, Vybhav A. Jetty, Ann T. Sweeney, Artem Astsaturov, Uyen Lam, Haoyang Wang, Karen Feghali
Publikováno v:
AACE Clinical Case Reports
AACE Clinical Case Reports, Vol 7, Iss 6, Pp 353-356 (2021)
AACE Clinical Case Reports, Vol 7, Iss 6, Pp 353-356 (2021)
Objective To report the first case, to our knowledge, of intermittent pancytopenia and cardiac tamponade occurring together in association with Autoimmune Addison's Disease (AAD). Methods A 21 year-old woman presented on three different occasions wit
Autor:
Saif Aasem, Assem M.
Publikováno v:
Endocrine Regulations, Vol 51, Iss 2, Pp 114-116 (2017)
A 31-year-old lady, diagnosed to have premature ovarian failure in the gynecology clinic, was referred for endocrine assessment because of an abnormal thyroid function test. Clinical examination revealed hypotension, and fungal skin infection under h
Externí odkaz:
https://doaj.org/article/bb33ce55c9dc480eb3c4bb861b7f8e68
Publikováno v:
Saudi Journal of Medicine and Medical Sciences, Vol 5, Iss 1, Pp 71-73 (2017)
A 25-year-old Saudi female with a known case of autoimmune thyroiditis presented to the Emergency Room in stuporous condition. A blood test revealed a blood sugar level of 1.7 mmols/l (30.6 mg/dl). The patient was resuscitated with intravenous glucos
Externí odkaz:
https://doaj.org/article/5e18a414d58149dabd34ebca9f35412c