Diagnosis of the clinical polymorphism of glucose-6-phosphate dehydrogenase deficiency in patients with hyperbilirubinemia

Two Azerbaijani families were examined to determine the nature of neonatal hyperbilirubinemia. Blood samples from neonatal infants with jaundice, their siblings, and parents were an object of this investigation. The pedigrees of the probands were compiled and analyzed. The levels of hemoglobin, red...

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Bibliographic Details
Main Author: G. A. Akperova
Format: Article
Language:Russian
Published: Ltd. “The National Academy of Pediatric Science and Innovation” 2016-03-01
Series:Rossijskij Vestnik Perinatologii i Pediatrii
Subjects:
Online Access:https://www.ped-perinatology.ru/jour/article/view/194