Splenic Artery Aneurysms, a Rare Complication of Type 1 Gaucher Disease: Report of Five Cases

Type 1 Gaucher disease is a rare genetic lysosomal disorder due to acid betaglucosidase deficiency. The main features are thrombocytopenia, anemia, hepatosplenomegaly and complex skeletal disease. Complications include pulmonary hypertension, cirrhosis and splenic infarction; comorbidities, such as...

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Detalles Bibliográficos
Autores principales: Serratrice, Christine, Cox, Timothy M., Leguy-Seguin, Vanessa, Morris, Elizabeth, Yousfi, Karima, Monnet, Olivier, Sibert, Annie, Allaham, Wassim, Belmatoug, Nadia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406779/
https://www.ncbi.nlm.nih.gov/pubmed/30744043
http://dx.doi.org/10.3390/jcm8020219

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406779/
https://www.ncbi.nlm.nih.gov/pubmed/30744043
http://dx.doi.org/10.3390/jcm8020219

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