Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Case Report / Olgu Sunumu"'
Publikováno v:
Turkish Archives of Pediatrics/Türk Pediatri Arşivi
Pott’s puffy tumor is a rare and serious complication of frontal sinusitis, characterized by the development of osteomyelitis and subperiostal abscess in the frontal bone. Paranasal sinus osteomas are benign osteoblastic tumors, usually seen in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aa8aa827787794864901506dbb8df346
http://europepmc.org/articles/PMC7750352
http://europepmc.org/articles/PMC7750352
Publikováno v:
Turkish Archives of Pediatrics/Türk Pediatri Arşivi
Bronchopulmonary dysplasia is a chronic lung disease that develops in low-birth-weight infants as a result of mechanical ventilation and oxygen toxicity in the early neonatal period. In these patients, mechanical ventilation and oxygen support are ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::419be35619e16a7067e1e574f386e99b
http://europepmc.org/articles/PMC7750334
http://europepmc.org/articles/PMC7750334
Autor:
Şengül, Özlem Kalaycık, Akkelle, Bilge Şahin, Volkan, Burcu, Tutar, Engin, Çelikel, Çiğdem A., Ertem, Deniz
Publikováno v:
Turkish Archives of Pediatrics/Türk Pediatri Arşivi
Sarcoidosis is a chronic multisystemic granulomatous disease that predominantly involves the thoracic lymph nodes and lungs and primarily occurs in young adults. Isolated extrapulmonary localization is uncommon in adults, and exceptionally rare in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::594b9c27b0e3ce195c25f7a854bb42bd
http://europepmc.org/articles/PMC7750332
http://europepmc.org/articles/PMC7750332
Publikováno v:
Turkish Archives of Pediatrics/Türk Pediatri Arşivi
Heterozygous inactivating mutations in the glucokinase gene cause the mildest form of maturity-onset diabetes of the adolescents. However, homozygous or compound heterozygous mutations in the glucokinase gene are a rare cause of permanent neonatal di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ae62aedc2fe37b342d0ae931207fec4
http://europepmc.org/articles/PMC7750344
http://europepmc.org/articles/PMC7750344
Publikováno v:
Turkish Archives of Pediatrics/Türk Pediatri Arşivi
Here we present two siblings, a 9-year-old boy and a 15-year-old girl at presentation, with congenital erythrocytosis due to an EPOR c.1316G>A (p.Trp439Term) mutation. The patients had nausea, abdominal pain, and headache when they presented with hem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d6c066b7df3be8b1fe2ee82ef8cfdef8
http://europepmc.org/articles/PMC7536457
http://europepmc.org/articles/PMC7536457
Autor:
Kutukculer, Necil, Boluk, Ezgi, Tokmeci, Nazan, Karaca, Neslihan Edeer, Azarsiz, Elif, Aksu, Guzide, Aykut, Ayca
Publikováno v:
Turkish Archives of Pediatrics/Türk Pediatri Arşivi
Purine nucleoside phosphorylase deficiency is one of the severe combined immunodeficiencies, which often clinically manifests with recurrent infections, neurologic symptoms and autoimmune diseases, and leads to thymocyte development and peripheral T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::67a137c3d44bb64d71e83a2dafc5024c
http://europepmc.org/articles/PMC7536453
http://europepmc.org/articles/PMC7536453
Publikováno v:
Turkish Archives of Pediatrics/Türk Pediatri Arşivi
Eosinophilic gastroenteritis is an inflammatory disease characterized by pathologic eosinophilic infiltration of any portion of the gastrointestinal tract. Depending on the involved site and layer of eosinophilic infiltration, symptoms and signs are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b59747e8f6356fb9c133437bc06e9ac
http://europepmc.org/articles/PMC7536449
http://europepmc.org/articles/PMC7536449
Publikováno v:
Turkish Archives of Pediatrics/Türk Pediatri Arşivi
Hypertrophic cardiomyopathy has the highest incidence rate among genetically inherited cardiac diseases. It develops as a result of mutations in genes in related to the sarcomere protein in cardiac muscle. Generally, this results in asymmetrical hype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5022ba0740b68115b17cb9eaca561eac
http://europepmc.org/articles/PMC7536448
http://europepmc.org/articles/PMC7536448
Publikováno v:
Turkish Archives of Pediatrics/Türk Pediatri Arşivi
Autoimmune pancreatitis has been described as a pancreatic manifestation of immunoglobulin G4-related disease, which is characterized by typical histopathologic, radiologic, and clinical features. Immunoglobulin G4-related disease is usually accompan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3ded89f159300e55ebe6fc1747dc10d3
http://europepmc.org/articles/PMC7344129
http://europepmc.org/articles/PMC7344129
Publikováno v:
Turkish Archives of Pediatrics/Türk Pediatri Arşivi
Neonatal diabetes mellitus is a monogenic disease that can present with hyperglycemia, dehydration, failure to thrive, and ketoacidosis within the first six months of life. Neonatal diabetes mellitus can be transient or permanent. Here, we describe a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39d096b5c19ac66f188e7b47933b06c0
http://europepmc.org/articles/PMC7344130
http://europepmc.org/articles/PMC7344130