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First clinical and genetic description of a family diagnosed with late-onset Pompe disease from Costa Rica
(2017)
Glycogen storage disease type II, also known as Pompe disease, is an autosomal recessive disorder caused by deficiency of enzymatic activity of acid alpha-glucosidase. The wide phenotypical variation of this disease relates ...
Spinal epidural empyema extending from a pleural empyema: case description and anatomical overview
(2017)
We present a case of a patient with diabetes with a pleural empyema originated from a pyomyositis process established after a central line procedure. This empyema later on extended into the spinal canal deriving into an ...
Pituitary apoplexy presenting as an intraventricular hemorrhage: An infrequent neurovascular emergency
(2017)
Pituitary macroadenomas may present with a pituitary apoplexy, commonly with associated hemorrhage, but
rarely large enough to show an intraventricular bleeding. This is a case report of a 66-year-old woman with a 3-
month ...