A neglected cause of recurrent rhabdomyolysis, LPIN1 gene defect: a rare case from TurkeyTurkish Journal of Pediatrics - Tập 62 Số 4 - Trang 647-651
Sevgi Topal, Melis Köse, Hasan Ağın, Ferhat Sarı, Mustafa Çolak, Gülhan Atakul, Utku Karaarslan, Rana İşgüder
Background. Rhabdomyolysis; can occur due to toxic, infectious, metabolic, and genetic causes. Severe rhabdomyolysis may progress to several clinical manifestations such as cardiac arrest and may pose a risk of mortality if it is not treated timely.
Case. In this article, we presented a 26-month-old patient who was admitted with an acute rhabdomyolysis attack and a venovenous he...... hiện toàn bộ
Pediatric langerhans cell histiocytosis: single center experience over a 17-year periodTurkish Journal of Pediatrics - Tập 58 Số 4 - Trang 349-355
Dilek İnce, Selcen Kundak, Yöntem Yaman, Serra Kamer, Yeşim Oymak, Ragıp Ortaç, Ayşe Erbay, Gülcihan Özek, Bengü Demirağ, Canan Vergin
This study aimed to analyze children with the diagnosis of Langerhans cell histiocytosis (LCH) who were diagnosed and treated between 1998-2015. Medical records were evaluated retrospectively for clinical and laboratory features, treatment details, and outcome. There were 20 patients, the median age of diagnosis was 37 months, M/F ratio: 1.5. Nine had single system (SS), 11 had multi...... hiện toàn bộ