Gaucher disease type 3 (Q84640): Difference between revisions
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A doença de Gaucher tipo 3 é a forma neurológica subaguda da doença de Gaucher (um distúrbio de armazenamento lisossômico causado por uma deficiência de glucocerebrosidase) caracterizada por encefalopatia progressiva e associada às manifestações sistêmicas (organomegalia, envolvimento ósseo, citopenia) de DG tipo 1 (ver este termo). | |||
| description / en | description / en | ||
Gaucher disease type 3 is the subacute neurological form of Gaucher disease (a lysosomal storage disorder caused by a deficiency in glucocerebrosidase) characterised by progressive encephalopathy and associated with the systemic manifestations (organomegaly, bone involvement, cytopenia) of GD type 1 (see this term). | |||
Revision as of 09:59, 15 August 2026
Gaucher disease type 3 is the subacute neurological form of Gaucher disease (a lysosomal storage disorder caused by a deficiency in glucocerebrosidase) characterised by progressive encephalopathy and associated with the systemic manifestations (organomegaly, bone involvement, cytopenia) of GD type 1 (see this term).
| Language | Label | Description | Also known as |
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| default for all languages | ID_312650726 |
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| English | Gaucher disease type 3 |
Gaucher disease type 3 is the subacute neurological form of Gaucher disease (a lysosomal storage disorder caused by a deficiency in glucocerebrosidase) characterised by progressive encephalopathy and associated with the systemic manifestations (organomegaly, bone involvement, cytopenia) of GD type 1 (see this term). |
