Hunter Syndrome in Northern India: Clinical features and Mutation Spectrum.

OBJECTIVE

To study the clinical profile and mutation spectrum of Hunter syndrome.

METHODS

Evaluation of 18 cases of Hunter syndrome from 17 families was done. Mutation analysis of Iduronate sulfatase (IDS) gene was done in 9 families, and mothers of four affected children with no family history.

RESULTS

Joint contracture, hepatomegaly and radiological changes were present in all children. 6 (33%) children had normal cognitive function at presentation. Point mutations were identified in all the 9 families for whom mutation analysis was done. Among 4 mothers tested from families without any family history, 2 (50%) were found to be carriers.

CONCLUSION

Accurate etiological diagnosis by mutation analysis of IDS gene is important in Hunter syndrome.