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