Griscelli syndrome: Report of a case and review of the literature

Pediatrics International

Volumn 43, Issue 3, 2001, Pages 298-301

  Kurugöl, Zafer ^a,b   Ozkinay, Ferda ^a   Vardar, Fadil ^a   Karaçali, Sabire ^a   Kutukçuler, Necil ^a   Deveci, Remziye ^a  

^a EGE UNIVERSITY   (Turkey)

^b EGE UNIVERSITY SCHOOL OF MEDICINE   (Turkey)

Author keywords

Griscelli syndrome; Immunodeficiency; Partial albinism

Indexed keywords

ANTIINFECTIVE AGENT; IMMUNOGLOBULIN;

ANTIMICROBIAL THERAPY; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CLINICAL FEATURE; ERYTHROCYTE TRANSFUSION; GRISCELLI SYNDROME; HUMAN; IMMUNE DEFICIENCY; LEUKOCYTE FUNCTION; MALE; NEUTROPHIL; NEWBORN; PIEBALDISM; PRIORITY JOURNAL; THROMBOCYTE TRANSFUSION;

FEMALE; GENES, RECESSIVE; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; INFANT; MALE; PIGMENTATION DISORDERS; SYNDROME;

EID: 0034946903     PISSN: 13288067     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1442-200X.2001.01383.x     Document Type: Article

References (10)

1. A syndrome associating partial albinism and immunodeficiency
2. Partial albinism with immunodeficiency (Griscelli syndrome)
3. Griscelli disease with cerebral involvement
4. Griscelli's syndrome: Clinical features of three siblings
5. Griscelli syndrome: Report of three cases
6. Assessment of neutrophil chemotaxis and random migration in children with thalassemia major
7. Familial erythrophagocytic lymphohistiocytosis
8. Chediak-Higashi syndrome
9. Partial albinism with immunodeficiency: Griscelli syndrome. Report of a case and review of the literature
10. Bone marrow transplantation (BMT) for the syndrome of pigmetary dilution and lymphohistiocytosis (Griscelli's syndrome)