Griscelli syndrome type 2; a pediatric case with immunodeficiency

Iranian Journal of Allergy, Asthma and Immunology

Volumn 6, Issue 3, 2007, Pages 155-157

  Tabatabaie, Parviz ^a,b   Mahjoub, Fatemeh ^a   Cheraghi, Taher ^a   Parvaneh, Nima ^a  

^a TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

Griscelli syndrome; Immunodeficiency; Phagocyte disorders

Indexed keywords

ANTIFUNGAL AGENT; CEFTAZIDIME; MELANIN; VANCOMYCIN;

ARTICLE; BLOOD EXAMINATION; BLOOD SMEAR; BONE MARROW BIOPSY; CASE REPORT; CHEST INFECTION; CLINICAL FEATURE; FEMALE; GRISCELLI SYNDROME; HOSPITAL ADMISSION; HUMAN; HUMAN TISSUE; IMMUNE DEFICIENCY; INFANT; LABORATORY TEST; MICROSCOPY; PEDIATRIC ADVANCED LIFE SUPPORT; SKIN COLOR;

FATAL OUTCOME; FEMALE; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; INFANT; PIGMENTATION DISORDERS; SYNDROME;

EID: 35848956292     PISSN: 17351502     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

1. Rosenzweig SD, Uzel G, Holland SM: Phagocyte Disorders. In: Stiehm ER, Ochs HD, Winkelstein JA. Immunologic Disorders in Infants and Children. USA. Saunders; 2004:618-51.
2. Griscelli syndrome, type 1, GS1: OMIM (online mendelian inheritance in man, Johns Hopkins University, viewed 5 Feb 2007, 〈http://www.ncbi.nlm.nih. gov/enterz/dispomin.cgi?id=214450〉.
3. Malhotra AK, Bhaskar G, Nanda M, Kabra M, Singh MK, Ramam M. Griscelli syndrome. J Am Acad Dermatol 2006; 55(2):337-40.
4. Westbroek W, Lambert J, Deschepper S, Kleta R, Bossche K, Seabra M, et al. Rab 27 b is UP-Regulated in Human Griscelli Syndrome Type II Melanocytes and linked to the Actin Cytoskelon via Exon F-Myosin Va Transcripts. Pigment Cell Res 2004; 17(5):498-505.
5. Aslan D, Sari S, Derinoz O, Dalgic B. Griscelli syndrome: description of a case with Rab27A mutation. Pediatr Hematol Oncol 2006; 23(3):255-61.