203-206 A Case With Microme.QXD
نویسنده
چکیده
A boy with no previous history of bleeding presented with ecchymoses and splenomegaly. He was followed up for thrombocytopenia and micromegakaryocytes for 20 months till clinically malignancy was diagnosed. Micromegakaryocytes must always be treated with suspicion, as they may provide an important clue for dyshematopoesis.
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Theoretical considerations of optimal conduit length for water transport in vascular plants
Summary 196 I. 196 1. The neglected dimension 196 2. Basic concepts 197 (a) The heuristic notion of vessel-tiers 197 (b) Ohm's law 199 (c) Conductances, resistances and resistivities 199 (d) Lumen and pit resistances 199 (e) The importance of conduit radius and length in conductance 199 II. 199 1. Nature and origin of xylem conduit...
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Apert syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynostosis, midfacial malformation and symmetrical syndactyly. We present a 10-month-old infant having all the features of classical Apert syndrome. How to cite this article: Khan S, Chatra L, Shenai P, Veena KM. Apert Syndrome: A Case Report. Int J Clin Pediatr Dent 2012; 5(3):203-206.
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