Open AccessFamilial Hemophagocytic Lymphohistiocytosis (Type 2) with solitary neurological presentation due to PRF1 gene mutation
Author(s) -
Namburu Sravanthi,
Saiprasad Onkareshwar Kavthekar,
Priti Bhimrao Kamble,
Anil Bapurao Kurane,
Rupali Naidu,
Vilas Maruti Jadhav
Publication year - 2022
Publication title -
ip international journal of medical paediatrics and oncology/ip international journal of medical paediatrics and oncology
Language(s) - English
Resource type - Journals
eISSN - 2581-4702
pISSN - 2581-4699
DOI - 10.18231/j.ijmpo.2022.030
Subject(s) - hepatosplenomegaly , hemophagocytic lymphohistiocytosis , pancytopenia , medicine , missense mutation , hypofibrinogenemia , immunology , pediatrics , leukodystrophy , mutation , pathology , disease , biology , genetics , gene , bone marrow , fibrinogen