Colonic Perforation in a Term Newborn with Hereditary Protein C Deficiency
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s13312-019-1690-4.pdf
Reference5 articles.
1. Miyata T, Sakata T, Zheng YZ, Tsukamoto H, Umeyama H, Uchiyama S, et al. Genetic characterization of protein C deficiency in Japanese subjects using a rapid and nonradioactive method for single-stand conformational polymorphism analysis and a model building. Thromb Haemost. 1996;76:302–11.
2. Theodoropoulou A, Koutroubakis IE. Ischemic colitis: clinical practice in diagnosis and treatment. World J Gastroenterol. 2008;14:7302–8.
3. Ahmed K, Darakhshan A, Au E, Khamashta MA, Katsoulis IE. Postpartum spontaneous colonic perforation due to antiphospholipid syndrome. World J Gastroenterol. 2009;15:502–5.
4. Kumagai K, Nishiwaki K, Sato K, Kitamura H, Yano K, Komatsu T, et al. Perioperative management of a patient with purpura fulminans syndrome due to protein C deficiency. Can J Anaesth. 2001;48:1070–4.
5. Ichiyama M, Inoue H, Ochiai M, Ishimura M, Shiraishi A, Fujiyoshi J, et al. Diagnostic challenge of the newborn patients with heritable protein C deficiency. J Perinatol. 2019;39:212–9.
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1. Stroke in a protein C‐deficient infant after stem cell transplant for CHARGE syndrome;Pediatric Blood & Cancer;2022-11-04
2. Compound heterozygous protein C deficiency with pulmonary embolism caused by a novel PROC gene mutation: Case report and literature review;Medicine;2022-10-21
3. Severe protein C deficiency in a newborn caused by a homozygous pathogenic variant in the PROC gene: a case report;BMC Pediatrics;2021-10-16
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