Indian pediatrics · 2016
Hunter Syndrome in Northern India: Clinical features and Mutation Spectrum.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Narayanan Dhanya Lakshmi, Srivastava Priyanka, Mandal Kausik, Gambhir Poonam Singh, Phadke Shubha R
Аннотация
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.
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.