Polycystic lipomembranous osteodysplasia - sclerosing leukoencephalopathy (Q98030): Difference between revisions
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Doença de Nasu-Hakola, também referida como osteodisplasia lipomembranosa policística com leucoencefalopatia esclerosante (PLOSL), é uma leucodistrofia rara hereditária caracterizada por demência pré-senil progressiva associada a fraturas ósseas recorrentes devido a lesões ósseas policísticas de extremidades inferiores e superiores. | |||
| description / en | description / en | ||
Nasu-Hakola disease, also referred to as polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL), is a rare inherited leukodystrophy characterised by progressive presenile dementia associated with recurrent bone fractures due to polycystic osseous lesions of the lower and upper extremities. | |||
Revision as of 14:17, 16 August 2026
Nasu-Hakola disease, also referred to as polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL), is a rare inherited leukodystrophy characterised by progressive presenile dementia associated with recurrent bone fractures due to polycystic osseous lesions of the lower and upper extremities.
| Language | Label | Description | Also known as |
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| default for all languages | ID_295989674 |
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| English | Polycystic lipomembranous osteodysplasia - sclerosing leukoencephalopathy |
Nasu-Hakola disease, also referred to as polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL), is a rare inherited leukodystrophy characterised by progressive presenile dementia associated with recurrent bone fractures due to polycystic osseous lesions of the lower and upper extremities. |
