Limits...
Clinicopathological features of adult-onset neuronal intranuclear inclusion disease

View Article: PubMed Central - PubMed

ABSTRACT

Neuronal intranuclear inclusion disease (NIID) has highly variable clinical manifestations. Sone et al. describe the clinical and pathological features of 57 adult-onset cases diagnosed by postmortem dissection/antemortem skin biopsy. They report ‘dementia dominant’ and ‘limb weakness’ subtypes, and recommend consideration of NIID in the differential diagnosis of leukoencephalopathy and neuropathy.

No MeSH data available.


Related in: MedlinePlus

Sporadic and familial NIID and phenotypic subgroup.
© Copyright Policy - cc-by
Related In: Results  -  Collection

License
getmorefigures.php?uid=PMC5382941&req=5

aww249-F5: Sporadic and familial NIID and phenotypic subgroup.

Mentions: As a consequence of this study, adult-onset NIID cases can be subgrouped into dementia-dominant and limb weakness-dominant phenotypes (Fig. 5).Figure 5


Clinicopathological features of adult-onset neuronal intranuclear inclusion disease
Sporadic and familial NIID and phenotypic subgroup.
© Copyright Policy - cc-by
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC5382941&req=5

aww249-F5: Sporadic and familial NIID and phenotypic subgroup.
Mentions: As a consequence of this study, adult-onset NIID cases can be subgrouped into dementia-dominant and limb weakness-dominant phenotypes (Fig. 5).Figure 5

View Article: PubMed Central - PubMed

ABSTRACT

Neuronal intranuclear inclusion disease (NIID) has highly variable clinical manifestations. Sone et al. describe the clinical and pathological features of 57 adult-onset cases diagnosed by postmortem dissection/antemortem skin biopsy. They report ‘dementia dominant’ and ‘limb weakness’ subtypes, and recommend consideration of NIID in the differential diagnosis of leukoencephalopathy and neuropathy.

No MeSH data available.


Related in: MedlinePlus