Non-neuronopathic Gaucher disease (Type I) in an elderly female: a case report
Early diagnosis of Gaucher disease is challenging due to its rarity and should be considered in patients presenting with hepatosplenomegaly, pancytopenia, and low glucocerebrosidase activity.
Authors
- Gopi Aryal (ORCID: https://orcid.org/0000-0002-8566-2593)
- Sujan Bohara (ORCID: https://orcid.org/0000-0003-3056-5283)
- Manoj Khadka (ORCID: https://orcid.org/0000-0002-0449-9254)
- Saubhagya Dhakal (ORCID: https://orcid.org/0009-0004-5873-1911)
- Samikshya Karki
- Deepak Ghimire (ORCID: https://orcid.org/0000-0002-8661-7938)
- Nahakul Poudel (ORCID: https://orcid.org/0009-0000-6717-4708)
- Sanjeet Bhattarai (ORCID: https://orcid.org/0000-0002-1957-1781)
Institutions
- Bir Hospital (NP)
- Nepal Development Research Institute (NP)
- Tribhuvan University Teaching Hospital (NP)
- Shahid Gangalal National Heart Centre (NP)
Publication Details
- Journal
- Annals of Medicine and Surgery
- Published
- 2024-09-10
- DOI
- https://doi.org/10.1097/ms9.0000000000002566
- Citations
- 1
- Primary Topic
- Lysosomal Storage Disorders Research
- Type
- article
- Field-Weighted Citation Impact
- 0.33