Acute treatment of hyperammonemia by continuous renal replacement therapy in a newborn patient with ornithine transcarbamylase deficiency

• Үндсэн зохиолчид: Hyo Jeong Kim (Зохиогч), Se Jin Park (Зохиогч), Kook In Park (Зохиогч), Jin Sung Lee (Зохиогч), Ho Sun Eun (Зохиогч), Ji Hong Kim (Зохиогч), Jae Il Shin (Зохиогч)
• Формат: Ном
• Хэвлэсэн: Korean Pediatric Society, 2011-10-01T00:00:00Z.
• Нөхцлүүд: article
• Онлайн хандалт: Connect to this object online.

Ornithine transcarbamylase (OTC) deficiency is well known as the most common inherited disorder of the urea cycle, and 1 of the most common causes of hyperammonemia in newborns. We experienced a case of a 3-day-old boy with OTC deficiency who appeared healthy in the first 2 days of life but develope...