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Mucopolysaccharidosis IVA: a novel splice acceptor site mutation in intron 4 of the N-acetylgalactosamine-6-sulfate sulfatase gene in an Afghanistan girl with classical Morquio disease.

Authors :
Fukuda S
Yamada N
Tomatsu S
Sukegawa K
Montaño AM
Hopwood JJ
Muller V
Orii T
Kondo N
Source :
The Japanese journal of human genetics [Jpn J Hum Genet] 1997 Jun; Vol. 42 (2), pp. 317-22.
Publication Year :
1997

Abstract

We report here a novel splice site mutation in intron 4 of the gene for N-acetylgalactosamine-6-sulfate sulfatase (GALNS) in an Afghanistan girl with severe mucopolysaccharidosis IVA (classical Morquio disease). Direct sequencing revealed a homozygous G to A transition in the conserved splice acceptor site in intron 4 (cagG-->caaG: designated IVS 4(-I) G-->A) which eliminates 144 nucleotides of exon 5 in her GALNS transcript and introduces an immediate premature termination codon (at Trp 141 of exon 4). The IVS 4(-1) G-->A has not been seen in other populations and this is the first report of the molecular basis of classical Morquio disease in an Afghanistan patient.

Details

Language :
English
ISSN :
0916-8478
Volume :
42
Issue :
2
Database :
MEDLINE
Journal :
The Japanese journal of human genetics
Publication Type :
Academic Journal
Accession number :
9290256
Full Text :
https://doi.org/10.1007/BF02766953