טוען...
Pitfalls in the diagnosis of Gaucher disease in Iraq: A diagnostic experience from a developing country
BACKGROUND AND OBJECTIVES: Gaucher disease (GD) is a rare hereditary disorder caused by deficiency of the lysosomal enzyme β-glucocerebrosidase. An early and definitive diagnosis minimizes the sequelae of misdiagnoses, and unnecessary and invasive diagnostic procedures. METHODS: A cross-sectional de...
שמור ב:
| הוצא לאור ב: | Pak J Med Sci |
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| Main Authors: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Professional Medical Publications
2021
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8155412/ https://ncbi.nlm.nih.gov/pubmed/34104165 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12669/pjms.37.3.2930 |
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