| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 4171927 | Paediatrics and Child Health | 2015 | 6 Pages | 
Abstract
												Hereditary spherocytosis is a red cell membrane disorder which is heterogeneous in respect to clinical presentation, biochemical and genetic basis. This review highlights the underlying pathophysiology, clinical features, investigations and management of HS in childhood.
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											Authors
												Sara Trompeter, May-Jean King, 
											