Gaucher's Disease in Albanian Children: Casuistics and Treatment

OBJECTIVE: Gaucher's disease is a rare genetic disorder that results in the accumulation of cerebrosides in the liver, spleen, kidneys, lungs, brain and bone marrow. The deficiency of the specific lysosomal enzyme glucocerebrosidase is considered as causative factor. The first effective treatme...

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Detalles Bibliográficos
Autores principales: Shehi, Behar, Boçari, Gëzim, Vyshka, Gentian, Xhepa, Rezar, Alushani, Dritan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2011
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446102/
https://www.ncbi.nlm.nih.gov/pubmed/23056756

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446102/
https://www.ncbi.nlm.nih.gov/pubmed/23056756

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