Cooperating G6PD mutations associated with severe neonatal hyperbilirubinemia and cholestasis
نویسندگان
چکیده
منابع مشابه
Severe neonatal hyperbilirubinemia leading to exchange transfusion
Background :Severe neonatal hyperbilirubinemia is associated with significant morbidity and mortality. This study was conducted to investigate the causes of severe hyperbilirubinemia leading to Exchange Transfusion (ET) from March 2009 to March 2011 in Bahrami children hospital, Tehran, Iran in order to establish guidelines to prevent profound jaundice & ET. Methods : 94 neonates underwent ...
متن کاملG6PD Enzyme Deficiency in Neonatal Pathologic Hyperbilirubinemia in Yazd
Abstract Background About 7.5% of the world population carries one or two deficient copy of glucose-6-phosphate dehydrogenase (G6PD) genes. According to WHO, its prevalence in Iran is 10 to 14.9%. This study aimed on determination of frequency of G6PD deficiency in neonates with jaundice who were hospitalized during 6 months (September 2008 to February 2009) in the city of Yazd, Iran. Materi...
متن کاملG6PD Enzyme Deficiency in Neonatal Pathologic Hyperbilirubinemia in Yazd
BACKGROUND About 7.5% of the world population carries one or two deficient copy of glucose-6-phosphate dehydrogenase (G6PD) genes. According to WHO, its prevalence in Iran is 10 to 14.9%. This study aimed on determination of frequency of G6PD deficiency in neonates with jaundice who were hospitalized during 6 months (September 2008 to February 2009) in the city of Yazd, Iran. MATERIALS AND ME...
متن کاملSevere neonatal hyperbilirubinemia leading to exchange transfusion
BACKGROUND Severe neonatal hyperbilirubinemia is associated with significant morbidity and mortality. This study was conducted to investigate the causes of severe hyperbilirubinemia leading to Exchange Transfusion (ET) from March 2009 to March 2011 in Bahrami children hospital, Tehran, Iran in order to establish guidelines to prevent profound jaundice & ET. METHODS 94 neonates underwent ET fo...
متن کاملErratum to: Neonatal Hyperbilirubinemia in infants with G6PD c.563C > T Variant
BACKGROUND There is a strong correlation between glucose-6-phosphate dehydrogenase (G6PD) deficiency and neonatal hyperbilirubinemia with a rare but potential threat of devastating acute bilirubin encephalopathy. G6PD deficiency was observed in 4-14% of hospitalized icteric neonates in Pakistan. G6PD c.563C > T is the most frequently reported variant in this population. The present study was ai...
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ژورنال
عنوان ژورنال: Pediatric Blood & Cancer
سال: 2010
ISSN: 1545-5009
DOI: 10.1002/pbc.22744