Dergiler / Turkish Journal of Medical Sciences / 2002 / Cilt: 32 - Sayı: 1

A Rare Case of Neonatal Hypotonia: Neonatal Nonketotic Hyperglycinemia

Sayfa
73–75
Yayın Tarihi
2022-11-05
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

NKH should be considered in a hypotonic newborn, especially if associated with acute deterioration, lethargy and seizures.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Hypotonia is a serious physical finding in a newborn infant.
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Temel Bulgular & Veri:Nonketotic hyperglycinemia (NKH) is a rare cause of neonatal hypotonia.
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Sonuç & Katkı:NKH should be considered in a hypotonic newborn, especially if associated with acute deterioration, lethargy and seizures.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Nonketotic hyperglycinemia · hypotonia. · Nonketotic hyperglycinemia

Özet

Hypotonia is a serious physical finding in a newborn infant. Nonketotic hyperglycinemia (NKH) is a rare cause of neonatal hypotonia. It is a defect of the glycine metabolism and has poor prognosis. We report a case of a newborn infant with NKH, presented with mild hypotonia and high creatine kinase values. NKH should be considered in a hypotonic newborn, especially if associated with acute deterioration, lethargy and seizures.

Abstract

Hypotonia is a serious physical finding in a newborn infant. Nonketotic hyperglycinemia (NKH) is a rare cause of neonatal hypotonia. It is a defect of the glycine metabolism and has poor prognosis. We report a case of a newborn infant with NKH, presented with mild hypotonia and high creatine kinase values. NKH should be considered in a hypotonic newborn, especially if associated with acute deterioration, lethargy and seizures.

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Bu Makaleye Atıf Yap

TAŞTEKİN, A., ÖRS, R., ÖZKAN, B., DENİZ, O. (2022). A Rare Case of Neonatal Hypotonia: Neonatal Nonketotic Hyperglycinemia. Turkish Journal of Medical Sciences, Cilt: 32 - Sayı: 1, 73–75. https://ajindex.com/articles/612203

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