A Case of Classical Galactosemia caused by Compound Heterozygous Mutations of the GALT Gene.
- Author:
Chong Kun CHEON
1
;
Min Sung CHO
;
Jung Min KO
;
Gu Hwan KIM
;
Han Wook YOO
Author Information
1. Department of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. hwyoo@amc.seoul.kr
- Publication Type:Case Report
- Keywords:
Classical galactosemia;
GALT-deficient;
GALT gene;
Heterozygous mutation
- MeSH:
Brain;
Diet;
Eye;
Female;
Galactose;
Galactosemias;
Galactosephosphates;
Hemorrhage;
Hepatomegaly;
Humans;
Infant;
Infant, Newborn;
Jaundice;
Jaundice, Obstructive;
Liver;
Neonatal Screening;
UTP-Hexose-1-Phosphate Uridylyltransferase
- From:Journal of Genetic Medicine
2008;5(2):131-135
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Classical galactosemia is an autosomal recessive disorder of galactose metabolism, caused by a deficiency of the enzyme galactose-1-phosphate uridyltransferase (GALT). Buildup of galactose-1-phosphate is toxic at high levels and can damage the liver, brain, eyes, and other vital organs. The case presented here was that of an 11-day-old female infant who had elevated galatose levels upon initial neonatal screening test with persistent cholestatic jaundice, coagulopathy, and hepatomegaly. The patient was transferred due to aggravation of clinical symptoms including bleeding and jaundice. She had a delayed galactose free diet because of an inappropriate diagnosis. We quickly provided her with a lactose/ galactose-restricted diet as per her final diagnosis. Clinical and laboratory results were improved after a few days of treatment. For confirmatory testing for classical galactosaemia, we simultaneously analyzed for GALT enzyme activity and allele-specific PCR/fragments for seven mutations and two polymorphisms in the GALT gene. We were able to find several GALT-deficient and compound heterozygous mutations of the GALT gene.
