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• W2954906573 startingPage "1475" @default.
• W2954906573 abstract "The most common lysosomal storage disorder is Gaucher disease (GD). It is a deficiency of lysosomal glucocerebrosidase (GBA) due to biallelic mutations in the GBA gene, characterized by the deposition of glucocerebroside in macrophage-monocyte system cells. The report targets clinical phenotypes of GD in order to correlate them with GBA gene mutations, as well as to identify GBA gene mutation in patients in Montenegro that are diagnosed with GD.Five patients (4 male, 1 female) of type 1 GD (GD1) are reported. The age at diagnosis ranged from 7 to 40. Patients experienced delays of 1-12 years in diagnosis after the original onset of symptoms. The most common mode of presentation was a variable degree of splenomegaly and thrombocytopenia, while other symptoms included bone pain, hepatomegaly, abdominal pain and fatigue. Osteopenia was present in a majority of the patients: 4/5. All patients were found to have an asymptomatic Erlenmeyer flask deformity of the distal femur. On enzyme replacement therapy (ERT), the hematological and visceral parameters showed significant improvement, but no significant progression in bone mineral density was noticed. GBA gene sequencing revealed homozygosity for the N370S mutation in one patient. The genotypes of the other patients were N370S/55bp deletion, N370S/D409H (2 patients), and H255Q/N370S (1 patient).The phenotypes of the GD1 encountered in Montenegro were severe but all responded well to ERT." @default.
• W2954906573 created "2019-07-12" @default.
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• W2954906573 date "2019-06-26" @default.
• W2954906573 modified "2023-09-23" @default.
• W2954906573 title "Gaucher disease in Montenegro - genotype/phenotype correlations: Five cases report" @default.
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• W2954906573 doi "https://doi.org/10.12998/wjcc.v7.i12.1475" @default.
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