Article
A neglected cause of recurrent rhabdomyolysis, LPIN1 gene defect: a rare case from Turkey.
The Turkish journal of pediatrics - 1 Jan 2020
Topal Sevgi, Köse Melis Demir, Ağın Hasan, Sarı Ferhat, Çolak Mustafa, Atakul Gülhan, Karaarslan Utku, İşgüder Rana
Abstract excerpt
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 hemodiafiltration (CVVHDF) was...
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