RT Journal Article
SR Electronic
T1 Neuronal intranuclear inclusion disease
JF Practical Neurology
JO Pract Neurol
FD BMJ Publishing Group Ltd
SP 246
OP 248
DO 10.1136/pn-2022-003582
VO 23
IS 3
A1 Kwan, Jia Rui
A1 Moy, Wai Lun
A1 Narasimhalu, Kaavya
A1 Yong, Kok Pin
YR 2023
UL http://pn.bmj.com/content/23/3/246.abstract
AB Neuronal intranuclear inclusion disease is a rare genetic condition, previously diagnosed only at postmortem, but its characteristic radiological features now allow its diagnosis in life. The clinical presentation is variable and we hope this case report will raise awareness of this condition.All data relevant to the study are included in the article or uploaded as online supplemental information.