A Different SLC2A1 Gene Mutation in Glut 1 Deficiency Syndrome: c.734A>C

Year 2017, Volume: 34 Issue: 6, 580 - 583, 01.11.2017

Rüya Çolak Senem Alkan Özdemir Ezgi Yangın Ergon Mehtap Kağnıcı Şebnem Çalkavur

https://izlik.org/JA68EA66LS

Abstract

Background: Glucose transporter type 1 deficiency
syndrome is the result of impaired glucose transport
into the brain. Patients with glucose transporter type
1 syndrome may present with infantile seizures,
developmental delay, acquired microcephaly, spasticity
and ataxia.
Case Report: Here, we report a rare case of glucose
transporter type 1 deficiency syndrome caused by a
different pathogenic variant in a 10-day-old neonate who
presented with intractable seizures and respiratory arrest.
Conclusion: This new pathogenic variant can be seen in
glucose transporter type 1 deficiency syndrome

Keywords

Glut 1 deficiency syndrome , neonatal seizures , mutation

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