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Recurrent pulmonary aspergillosis and mycobacterial infection in an unsplenectomized patient with type 1 Gaucher disease

BACKGROUND: The clinical presentation of Gaucher disease (GD), an inherited lysosomal storage disorder caused by the deficient activity of the lysosomal enzyme glucocerebrosidase, is highly variable, and three clinical types are distinguished based upon the presence of neurologic symptoms. Thrombocy...

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Библиографические подробности
Главные авторы: Machaczka, Maciej, Lorenz, Fryderyk, Kleinotiene, Grazina, Bulanda, Agnieszka, Markuszewska-Kuczyńska, Alicja, Raistenskis, Juozas, Klimkowska, Monika
Формат: Artigo
Язык:Inglês
Опубликовано: Informa Healthcare 2014
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Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC3916717/
https://ncbi.nlm.nih.gov/pubmed/24195576
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3109/03009734.2013.857373
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