I would like to have most probable diagnosis of an infant (3mnths) with persistent anemia(requiring regular transfusions since birth) failure to thrive, delayed development, only hepatomegaly on examination, candidiasis, with history of 3 sibling deaths at 3-6 months of life, consanguinous marriage of parents.. following investigations were normal- TORCH, HIV, BONE MARROW ASPIRATION, THALASSEMIA PROFILE (except low serum iron), SKELETAL SURVEY, ONLY LFT's WERE DERANGED with hypoalbuminemia, raised SGPT.
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