Craniopharyngioma in boy suffering from chronic granulomatous disease – case report

Abstract

CGD is an inherited (X chromosomal or autosomal recessive) primary immunodeficiency regarding functional disturbance of phagocytes which lead to the severe recurrent bacterial and fungal infection observed since birth. Manifestations of CGD including central nervous system are less common. This case report emphasizes the diagnostic and therapeutic problems… (More)

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@inproceedings{POLASKA2009CraniopharyngiomaIB, title={Craniopharyngioma in boy suffering from chronic granulomatous disease – case report}, author={BO ̄ENA POLA{\~N}SKA and Aleksandra Lewandowicz-Uszyńska and Adam Jankowski}, year={2009} }