Ghosal Hematodiaphyseal Dysplasia with Myelofibrosis
- 15 September 2012
- journal article
- case report
- Published by Springer Science and Business Media LLC in Indian Journal of Pediatrics
- Vol. 80 (12), 1050-1052
- https://doi.org/10.1007/s12098-012-0872-z
Abstract
Diaphyseal dysplasia with refractory anemia requiring blood transfusion is a relatively new entity having possible autosomal recessive inheritance. Prednisolone therapy alleviates the need for repeated transfusion. One such case is being reported here.Keywords
This publication has 9 references indexed in Scilit:
- Ghosal hematodiaphyseal dysplasia: A rare cause of a myelophthisic anemiaPediatric Blood & Cancer, 2010
- Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome)Nature Genetics, 2008
- Ghosal type hemato-diaphyseal dysplasia: A rare variety of Engelmann’s diseaseIndian Journal of Pediatrics, 2007
- A gene responsible for Ghosal hemato-diaphyseal dysplasia maps to chromosome 7q33–34Human Genetics, 2007
- Un nouveau cas de dysplasie hématodiaphysaire de GhosalArchives de Pédiatrie, 2005
- Ghosal haemato-diaphyseal dysplasia: A new disorderEuropean Journal of Pediatrics, 1993
- Diaphyseal dysplasia [corrected] with anemia and thrombocytopenia.1989
- High-dose intravenous methylprednisolone therapy for anemia associated with diaphyseal dysplasiaThe Journal of Pediatrics, 1989
- Diaphyseal dysplasia associated with anemiaThe Journal of Pediatrics, 1988