Identification of a novel mutation of AGL gene in two siblings affected with glycogen storage disease type IIIa.
- Author:
Li GUO
1
;
Weixia LIN
;
Man MAO
;
Yuanzong SONG
Author Information
- Publication Type:Journal Article
- MeSH: Adolescent; Amino Acid Sequence; Female; Glycogen Debranching Enzyme System; genetics; Glycogen Storage Disease Type III; genetics; Humans; Infant; Male; Mutation; genetics; Siblings
- From: Chinese Journal of Medical Genetics 2017;34(4):499-503
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo detect potential mutation of the AGL gene in two siblings affected with glycogen storage disease type IIIa.
METHODSClinical data of the two siblings was collected and analyzed. Genomic DNA was extracted from peripheral venous blood samples from the patients and their parents. All exons and their flanking sequences of the AGL gene were subjected to PCR amplification and Sanger sequencing. Suspected mutation was verified in 75 healthy controls.
RESULTSThe main clinical features of the two siblings included hypoglycemia and hepatomegaly, along with markedly elevated liver and myocardial enzymes. Genetic analysis revealed that both siblings harbored compound heterozygous mutations c.1735+1G>T and c.959-1G>C of the AGL gene. Among these, the splicing mutation c.959-1G>C was a novel one with an allele frequency of <1%.
CONCLUSIONBased on their clinical features and genetic analysis, the siblings were diagnosed with glycogen storage disease type IIIa. The c.959-1G>C has enriched the spectrum of AGL gene mutations.
