Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/132153
Title: Griscelli syndrome - the commonest cause of Haemophagocytic Lymphohistiocytosis in Maltese children
Authors: Ellul, M.
Calvagna, Victor
Said, Edith
Cuschieri, Alfred
Keywords: Newborn infants -- Diseases
Newborn infants -- Malta -- Case studies
Rare diseases -- Diagnosis
Lymphohistiocytosis, hemophagocytic
Issue Date: 2006
Publisher: University of Malta. Medical School
Citation: Ellul, M., Calvagna , V., Said, E., & Cuschieri, A. (2006). Aicardi-Goutières syndrome: a genetic syndrome mimicking congenital infection – a description of two new cases. Malta Medical Journal, 18(Supplement), 70.
Abstract: Aims: The presentation will describe the clinical features, laboratory findings, diagnostic criteria and treatment modalities of children with the Griscelli syndrome and Haemophagocytic Lymphohistiocytosis who presented to the Department of Paediatrics in Malta from 2005 to 2006. Methods: Three short case presentations will be followed by a description of the Griscelli syndrome and Haemophagocytic Lymphohistiocytosis.
URI: https://www.um.edu.mt/library/oar/handle/123456789/132153
ISSN: 18133339
Appears in Collections:Scholarly Works - FacM&SAna

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