Hemophagocytic Lymphohistiocytosis Griscelli Syndrome Presented with Status Epilepticus and

References (3)

1. Patıroğlu T, Özdemir MA, Patıroğlu TE. Griscelli’s syndrome: clinical and immunological features of two siblings. Turk J Hematol 2000;17:85-87.
2. Dotta L, Parolini S, Prandini A, Tabellini G, Antolini M, Kingsmore SF, Badolato R. Clinical, laboratory and molecular signs of immunodeficiency inpatients with partial oculo-cutaneous albinism. Orphanet J Rare Dis 2013;8:168. Aslan D, Sari S, Derinöz O, Dalgiç B. Griscelli syndrome: description of a case with Rab27A mutation. Pediatr Hematol Oncol 2006;23:255-261.
3. Meeths M, Bryceson YT, Rudd E, Zheng C, Wood SM, Ramme K, Beutel K, Hasle H, Heilmann C, Hultenby K, Ljunggren HG, Fadeel B, Nordenskjöld M, Henter JI. Clinical presentation of Griscelli syndrome type 2 and spectrum of RAB27A mutations. Pediatr Blood Cancer 2010;54:563-572.