Griscelli syndrome subtype 2 with hemophagocytic lympho-histiocytosis: A case report and review of literature-Reference-Cited by-同舟云学术

Griscelli syndrome subtype 2 with hemophagocytic lympho-histiocytosis: A case report and review of literature

Published:2017 Issue:1 Volume:6 Page:76-79
ISSN:2186-361X
Container-title:Intractable & Rare Diseases Research
language:en
Short-container-title:IRDR

Author:

Minocha Priyanka¹,Choudhary Richa¹,Agrawal Anika¹,Sitaraman Sadasivan¹

Affiliation:

1. Department of Pediatrics, Sawai Man Singh Medical College and Hospital

Publisher

International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)

Subject

General Medicine

Link

https://www.jstage.jst.go.jp/article/irdr/6/1/6_2016.01084/_pdf

Reference11 articles.

1. 1. Singh A, Garg A, Kapoor S, Khurana N, Entesarian M, Tesi B. An Indian boy with griscelli syndrome type 2: Case report and review of literature. Indian J Dermatol. 2014; 59:394-397.

2. 2. Mahalingashetti PB, Krishnappa MH, Kalyan PS, Subramanian RA, Padhy S. Griscelli sndrome: Hemophagocytic lymphohistiocytosis with silvery hair. J Lab Physicians. 2012; 4:129-130.

3. 3. Rajyalakshmi R, Chakrapani RN. Griscelli syndrome type 2: A rare and fatal syndrome in a South Indian boy. Indian J Pathol Microbiol. 2016; 59:113-116.

4. 4. Griscelli C, Durandy A, Guy-Grand D, Daguillard F, Herzog C, Prunieras M. A syndrome associating partial albinism and immunodeficiency. Am J Med. 1978; 65: 691-702.

5. 5. Dotta L, Parolini S, Prandini A, Tabellini G, Antolini M, Kingsmore SF, Badolato R. Clinical, laboratory and molecular signs of immunodeficiency in patients with partial oculo-cutaneous albinism. Orphanet J Rare Dis. 2013; 8:168.

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