Long‐term follow‐up following bone marrow transplantation for Hunter disease
- 1 June 1999
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 22 (5), 638-648
- https://doi.org/10.1023/a:1005525931994
Abstract
Bone marrow transplantation (BMT) was performed in 10 patients with Hunter disease (mucopolysaccharidosis type II, iduronate‐2‐sulphatase deficiency). The donor was an HLA‐identical sibling in 2 case...Keywords
This publication has 25 references indexed in Scilit:
- Mutation analysis in 20 patients with Hunter diseaseHuman Mutation, 1996
- Bone marrow transplantation in Hunter syndrome (mucopolysaccharidosis type II): two-year follow-up of the first Italian patient and review of the literature.1995
- Molecular genetics of muccpolysaccharidosis type I: Diagnostic, clinical, and biological implicationsHuman Mutation, 1995
- Long-term follow-up of a patient transplanted for Hunter's disease type IIB: a case report and literature review.1994
- Female twin with hunter disease due to nonrandom inactivation of the X‐chromosome: A consequence of twinningAmerican Journal of Medical Genetics, 1992
- Rising IQ Scores in British Children: Recent EvidenceJournal of Child Psychology and Psychiatry, 1992
- THE NATURAL HISTORY OF THE SEVERE FORM OF HUNTER'S SYNDROME: A STUDY BASED ON 52 CASESDevelopmental Medicine and Child Neurology, 1983
- A clinical and genetic study of Hunter's syndrome. 1 HeterogeneityJournal of Medical Genetics, 1982
- A clinical and genetic study of Hunter's syndrome. 2 Differences between the mild and severe formsJournal of Medical Genetics, 1982
- Mild form of Hunter's syndrome: clinical delineation based on 31 cases.Archives of Disease in Childhood, 1982