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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Detalles Bibliográficos
Autores principales: Machaczka, Maciej, Lorenz, Fryderyk, Kleinotiene, Grazina, Bulanda, Agnieszka, Markuszewska-Kuczyńska, Alicja, Raistenskis, Juozas, Klimkowska, Monika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Informa Healthcare 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3916717/
https://www.ncbi.nlm.nih.gov/pubmed/24195576
http://dx.doi.org/10.3109/03009734.2013.857373

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3916717/
https://www.ncbi.nlm.nih.gov/pubmed/24195576
http://dx.doi.org/10.3109/03009734.2013.857373

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