A Newborn Infant With Poor Feeding: Non-ketotic Hyperglycinemia

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 oth...

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Bibliographic Details
Main Authors: Masoumeh Ghesmati, Alireza Jashni Motlagh
Format: Article
Language:English
Published: Alborz University of Medical Sciences 2019-12-01
Series:International Journal of Enteric Pathogens
Subjects:
Online Access:http://enterpathog.abzums.ac.ir/PDF/ijep-4288

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