Abstract:
:Neuronal intranuclear inclusion disease (NIID) is a progressive, usually fatal degenerative neurologic condition characterized by eosinophilic, intranuclear inclusions in neurons of the central and peripheral nervous system. We report a boy with onset of disease manifestations at age 3 and death at age 9, who showed clinical and pathologic findings characteristic of NIID. The case is unique because of cardiomyopathy manifested 1 year prior to death. Postmortem findings confirmed the presence of cardiomyopathy and revealed intranuclear inclusions in myocytes. Neither nuclear inclusions in the myocardium nor cardiac involvement have previously been reported in NIID.
journal_name
Hum Patholjournal_title
Human pathologyauthors
Oyer CE,Cortez S,O'Shea P,Popovic Mdoi
10.1016/0046-8177(91)90296-2subject
Has Abstractpub_date
1991-07-01 00:00:00pages
722-4issue
7eissn
0046-8177issn
1532-8392pii
0046-8177(91)90296-2journal_volume
22pub_type
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