Two Novel Missense Mutations in Nonketotic Hyperglycinemia
Journal of Child Neurology, cilt.30, sa.6, ss.789-792, 2015 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 30 Sayı: 6
- Basım Tarihi: 2015
- Doi Numarası: 10.1177/0883073814535499
- Dergi Adı: Journal of Child Neurology
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.789-792
- Anahtar Kelimeler: nonketotic hyperglycinemia, novel, mutation, T-PROTEIN GENE, FAMILIES, GLDC, AMT
- Lokman Hekim Üniversitesi Adresli: Hayır
Özet
© The Author(s) 2014.Nonketotic hyperglycinemia (OMIM no. 605899) is an autosomal recessively inherited glycine encephalopathy, caused by a deficiency in the mitochondrial glycine cleavage system. Here we report 2 neonates who were admitted to the hospital with complaints of respiratory failure and myoclonic seizures with an elevated cerebrospinal fluid/plasma glycine ratio and diagnosed as nonketotic hyperglycinemia. We report these cases as 2 novel homozygous mutations; a missense mutation c.593A>T (p.D198 V) in the glycine decarboxylase gene and a splicing mutation c.339G>A (Q113Q) in the aminomethyltransferase gene were detected. We would like to emphasize the genetic difference of our region in inherited metabolic diseases once again.