Deletion of exon 4 in the N-acetylgalactosamine-4-sulfatase gene in a Taiwanese patient with mucopolysaccharidosis type VI.

Abstract

Mucopolysaccharidosis type VI (MPS VI) is a rare autosomal recessive disorder caused by a deficiency of N-acetylgalactosamine-4-sulfatase (ARSB), one of the enzymes required for the degradation of dermatan sulfate (DS). Accumulation of DS in connective tissue causes growth failure, resulting in short stature. Here, we observed a 5-year-old girl who was the only one affected member of her family and who presented with an exaggerated, convex curvature of the back at the age of one year. Abnormal excretion of DS in the urine and extremely low leukocyte ARSB activity were noted. The patient was suspected to have MPS VI. Direct DNA sequencing indicated that there was no mutation in the coding region of ARSB. However, RT-PCR analysis of RNA prepared from blood samples indicated the deletion of the entire exon 4. Further analysis of the genomic DNA by quantitative PCR confirmed a homozygous deletion of exon 4, an unusual intragenic deletion in ARSB. The deletion led to a truncated protein that lacks most of the catalytic domain. The patient received recombinant human ARSB as enzyme replacement therapy (ERT) at an early stage (2 years), and responded positively in terms of skeletal development and other developmental milestones. The early identification of type VI MPS patients and subsequent treatment with ERT may be beneficial for the clinical outcome of MPS VI patients. In addition, detailed gene analysis may enhance the ability to provide genetic counseling to families of patients affected by MPS VI.

• Authors: Wei-De Lin, Yu-Yuan Ke, I-Ching Chou, Chung-Hsing Wang, Fuu-Jen Tsai
• Journal: The Tohoku journal of experimental medicine (Tohoku J Exp Med) Vol. 235 Issue 4 Pg. 267-73 (04 2015) ISSN: 1349-3329 [Electronic] Japan
• PMID: 25797215 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• RNA, Messenger
• DNA
• N-Acetylgalactosamine-4-Sulfatase

Topics

• Asian People (genetics)
• Base Sequence
• Child, Preschool
• DNA (genetics)
• Exons (genetics)
• Family
• Female
• Gene Dosage
• Genome, Human
• Humans
• Male
• Molecular Sequence Data
• Mucopolysaccharidosis VI (enzymology, genetics)
• N-Acetylgalactosamine-4-Sulfatase (chemistry, genetics)
• Pedigree
• RNA, Messenger (genetics, metabolism)
• Sequence Deletion (genetics)
• Taiwan