how to cite this article: razzaghy azar m. approach to hereditary storage diseases in patients with hepatosplenomegaly. iran j child neurol. 2015 autumn;9:4(suppl.1): 18-19.   pls see pdf.

1Assistant Professor, Internal Medicine; 2Assistant Professor, Pathology; 3Head of Department of Critical Care; Military Hospital, Trivandrum Received: 22.07.2011; Accepted: 10.08.2013 Sir, T e C a s e r e p o r t “ M u l t i p l e m y e l o m a p r e s e n t i n g w i t h hepatosplenomagaly”1 was interesting and we would l ike to o f fer these comments 1. Peripheral blood smear giving a clue t...

Tuberculosis is a serious public health issue in developing countries. Hypercalcemia, though reported granulomatous disease, mild and asymptomatic tuberculosis. A 16 year old girl female presented with significant weight loss, loss of appetite on examination hepatosplenomegaly. Ultrasound abdomen (USG) showed mesenteric retroperitoneal lymphadenopathy hepatosplenomegaly ascites. We report an un...