Articles on neonate

ALİ ANNAGÜR, HÜSEYİN ALTUNHAN, RAHMİ ÖRS

2011, Vol 27, Issue 4, Page 255-259

Neonatal hemochromatosis is a rare disease clinically defined as severe neonatal liver disease in association with extrahepatic siderozis. The etiology of neonatal hemochromatosis is not understood exactly. However, according to a theory neonatal hemochromatosis is accepted to be an alloimmune...

NİLÜFER GÜZOĞLU, BİRGÜL SAY, NURDAN URAS, UĞUR DİLMEN

2014, Vol 30, Issue 3, Page 137-138

Very long-chain fatty acid dehydrogenase (VLCAD) deficiency is an autosomal recessive disorder of mitochondrial fatty acid oxidation. Elevated plasma level of acyl-carnitine by Tandem mass spectrometry prompts the diagnosis of VLCAD. We herein report a neonate with a diagnosis of VLCAD whose...

NURİYE EMİROĞLU, MURAT KONAK, TAMER ALTINOK, SEVGİ PEKCAN, KEMAL ÖDEV, RAHMİ ÖRS

2016, Vol 32, Issue Ek, Page 59-61

Congenital lobar emphysema (CLE) is a rare anomaly of lung development that presents in the neonatal period. A 13-day-old girl baby was admitted to our unit because of primary pulmonary hypoplasia. She had presented with severe dyspnea and cyanosis, where chest radiograph and chest computed...

SELVİ GÜLAŞI, ÜMİT ÇELİK

2018, Vol 34, Issue 1, Page 40-50

Invasive candidiasis is responsible for about 10% of nosocomial sepsis and it continues to be significant cause of serious morbidity and mortality in very low birth weight infants. Alhough the informations about the antifungal drugs which used for Candida species are increasing, studies and...