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Griscelli syndrome

Authors:	Sanjeev?Rath,Vivek?Jain,R.?K.?Marwaha author-information" > author-information__contact u-icon-before" > mailto:rammarwaha@rediffmail.com" title=" rammarwaha@rediffmail.com" itemprop=" email" data-track=" click" data-track-action=" Email author" data-track-label=" " >Email author,Amita?Trehan,L.?S.?Rajesh,Vijay?Kumar

Affiliation:	(1) department of Pathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India;(2) I/CDivision of Pediatric Hematology and Oncology, Advanced Pediatric Centre, Postgraduate Institute of Medical Education and Research, 160012 Chandigarh, India

Abstract:	An eight month old male infant presented with recurrent infections and partial albinism. Initially a possibility of Chediak Higashi syndrome (CHS) was considered, but a negative investigative work up prompted us to look for an alternate diagnosis. A literature search revealed that Griscelli syndrome (GS) has overlapping symptoms and signs. The findings in skin and hair biopsies in Griscelli syndrome are distinctive.

Keywords:	Partial albinism Pigmentary dilution Hemophagocytosis Immuno-deficiency
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