The Evaluation of Skeletal Manifestations in Patients with Gaucher Disease
Aim:Gaucher disease (GD) is the most prevalent hereditary lysosomal storage disorder, affecting multiple organ systems. It is characterized by a deficiency of the enzyme glucocerebrosidase leading to an accumulation of glucosylceramide in lysosomes. The majority of patients present with hepatospleno...
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| Principais autores: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Ege University, Faculty of Medicine, Department of Pediatrics and Ege Children Foundation
2021-09-01
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| Series: | Journal of Pediatric Research |
| Assuntos: | |
| Acceso en liña: |
http://jpedres.org/archives/archive-detail/article-preview/the-evaluation-of-skeletal-manifestations-in-patie/48640
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