A Newborn Infant With Poor Feeding: Non-ketotic Hyperglycinemia

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Ghesmati Masoumeh; Jashni Motlagh Alireza

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Journal Paper

Paper Information

Journal: International Journal of Enteric Pathogens Year:2019 | Volume:7 | Issue:4 Page(s): 134-136

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Title

A Newborn Infant With Poor Feeding: Non-ketotic Hyperglycinemia

Author(s)

Ghesmati Masoumeh | Jashni Motlagh Alireza | Issue Writer Certificate

Keywords

Non-ketotic hyperglycinemia

Neonate

Hypotonia

Abstract

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 and poor feeding. The neonatal-onset NKH was diagnosed based on a markedly elevated cerebrospinal fluid/plasma glycine ratio of 0. 32 and confirmed by the genetic test. It is extremely rare that NKH is manifested with poor feeding and Hypotonia thus considering this diagnosis in infants with poor feeding and Hypotonia is highly important.

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APA: Copy

Ghesmati, Masoumeh, & Jashni Motlagh, Alireza. (2019). A Newborn Infant With Poor Feeding: Non-ketotic Hyperglycinemia. INTERNATIONAL JOURNAL OF ENTERIC PATHOGEN, 7(4), 134-136. SID. https://sid.ir/paper/766940/en

Vancouver: Copy

Ghesmati Masoumeh, Jashni Motlagh Alireza. A Newborn Infant With Poor Feeding: Non-ketotic Hyperglycinemia. INTERNATIONAL JOURNAL OF ENTERIC PATHOGEN[Internet]. 2019;7(4):134-136. Available from: https://sid.ir/paper/766940/en

IEEE: Copy

Masoumeh Ghesmati, and Alireza Jashni Motlagh, “A Newborn Infant With Poor Feeding: Non-ketotic Hyperglycinemia,” INTERNATIONAL JOURNAL OF ENTERIC PATHOGEN, vol. 7, no. 4, pp. 134–136, 2019, [Online]. Available: https://sid.ir/paper/766940/en

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