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Review Article Open Access
Galactosemia is an autosomal recessive inherited disease of the galactose metabolism developing depending on galactose-1-phosphate uridyl transferase deficiency. In this report, a newborn galactosemia case with abnormal presentation has been presented. Hepatic and renal functions of the infants diagnosed with ammonia increase in newborn or early infancy period should be revised rapidly and the treatment should be started immediately.
Newborn, Galactosemia, Liver failure, Contraceptives, Barrier Contraceptives, Behavioral Contraceptives, Birth Control, Contraception, Dual Protection Contraceptives, Emergency Contraceptives, Family Planning, Fertility Control, Hormonal Contraceptives, Implantable Contraceptives, Intrauterine Devices, Sex Education, Sexually Transmitted Infections, Sterilization, Tubal Ligation, Vasectomy, Reproductive Physiology, Prenatal Diagnosis