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Gaucher disease and β-thalassemia: A rare coinheritance.
- Source :
-
Blood cells, molecules & diseases [Blood Cells Mol Dis] 2017 Jun; Vol. 65, pp. 35-37. Date of Electronic Publication: 2017 Apr 21. - Publication Year :
- 2017
- Subjects :
- Child
Enzyme Replacement Therapy methods
Gaucher Disease diagnostic imaging
Gaucher Disease genetics
Gaucher Disease therapy
Glucosylceramidase therapeutic use
Hepatomegaly diagnostic imaging
Hepatomegaly genetics
Hepatomegaly therapy
Humans
Magnetic Resonance Imaging
Male
Mutation
Splenomegaly diagnostic imaging
Splenomegaly genetics
Splenomegaly therapy
beta-Globins genetics
beta-Thalassemia diagnostic imaging
beta-Thalassemia genetics
beta-Thalassemia therapy
Gaucher Disease complications
Hepatomegaly complications
Paternal Inheritance
Splenomegaly complications
beta-Thalassemia complications
Subjects
Details
- Language :
- English
- ISSN :
- 1096-0961
- Volume :
- 65
- Database :
- MEDLINE
- Journal :
- Blood cells, molecules & diseases
- Publication Type :
- Report
- Accession number :
- 28458077
- Full Text :
- https://doi.org/10.1016/j.bcmd.2017.04.007