Polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly

MONDO:0009092

A rare inherited leukodystrophy characterized by progressive presenile dementia associated with recurrent bone fractures due to polycystic osseous lesions of the lower and upper extremities.

Also known as: NHD, Nasu-Hakola disease, PLO-SL, PLOSL, polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy, polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly, brain-bone-fat disease, dementia, prefrontal, with bone cysts

0 clinical trials for this condition and its sub-types, 0 tagged with Polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal recessive disease (999) ↑ Leukodystrophy (72) ↑ Primary osteolysis (5)

Sub-types of Polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly

Including sub-types (0) Tagged with Polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.