Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III.

Abstract

Glycogen storage disease type III (GSD III) is an autosomal recessive inborn error of metabolism caused by mutations in the glycogen debranching enzyme amylo-1,6-glucosidase gene, which is located on chromosome 1p21.2. GSD III is characterized by the storage of structurally abnormal glycogen, termed limit dextrin, in both skeletal and cardiac muscle and/or liver, with great variability in resultant organ dysfunction. The spectrum of AGL gene mutations in GSD III patients depends on ethnic group. The most prevalent mutations have been reported in the North African Jewish population and in an isolate such as the Faroe Islands. Here, we present the molecular and biochemical analyses of 22 Tunisian GSD III patients. Molecular analysis revealed three novel mutations: nonsense (Tyr1148X) and two deletions (3033_3036del AATT and 3216_3217del GA) and five known mutations: three nonsense (R864X, W1327X and W255X), a missense (R524H) and an acceptor splice-site mutation (IVS32-12A>G). Each mutation is associated to a specific haplotype. This is the first report of screening for mutations of AGL gene in the Tunisian population.

• Authors: Amira Mili, Ilhem Ben Charfeddine, Ons Mamaï, Sonia Abdelhak, Labiba Adala, Abdelbasset Amara, Serena Pagliarani, Sabrina Lucchiarri, Sabrina Lucchiari, Abdelkarim Ayadi, Neji Tebib, Abdelaziz Harbi, Jihene Bouguila, Dorra H'Mida, Ali Saad, Khalifa Limem, G P Comi, Moez Gribaa
• Journal: Journal of human genetics (J Hum Genet) Vol. 57 Issue 3 Pg. 170-5 (Mar 2012) ISSN: 1435-232X [Electronic] England
• PMID: 22089644 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Glycogen Debranching Enzyme System
• amylo-1,6-glucosidase

Topics

• Adolescent
• Black People (genetics)
• Child
• Child, Preschool
• Female
• Glycogen Debranching Enzyme System (genetics)
• Glycogen Storage Disease Type III (diagnosis, genetics)
• Haplotypes
• Humans
• Infant
• Male
• Mutation
• Polymorphism, Single Nucleotide
• Tunisia