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A Newborn Infant With Poor Feeding: Non-ketotic Hyperglycinemia
2019
International Journal of Enteric Pathogens
Non-ketotic hyperglycinemia (NKH) is a rare autosomal recessive disorder affecting glycine metabolism that is a rare metabolic disorder in infants. The clinical manifestations of poor sucking, hypotonicity, lethargy, hiccups, and seizures develop within six hours to eight days of the birth of an otherwise healthy newborn. The present study introduced a newborn girl with poor feeding and hypotonia in the first day after birth with NKH. In addition, the patient was evaluated regarding hypotonia
doi:10.15171/ijep.2019.28
fatcat:cafrmhx7mbacviy5kq2ul27e6u