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- Dalveer Singh, Charlie Chia-Tsong Hsu, Gigi Nga Chi Kwan, and Ipeson Korah.
- Department of Medical Imaging, The Townsville Hospital, Douglas, Queensland, Australia.
- J Neuroimaging. 2015 Nov 1; 25 (6): 1038-43.
AbstractPontine tegmental cap dysplasia (PTCD) is recently recognized as a rare congenital brain stem malformation with typical neuroimaging hallmarks of ventral pontine hypoplasia and vaulted pontine tegmentum projecting into the fourth ventricle. PTCD patients also demonstrate variable cranial neuropathy with predilection for involvement of the vestibulocochlear and facial nerves. We present a case of PTCD diagnosed on MRI in the neonatal period. During early infancy, the patient displayed features of multiple cranial neuropathies and bilateral hearing loss. At the age of 2, the patient underwent further MRI assessment with dedicated high resolution T2 SPACE sequence to delineate the cranial nerve deficiencies.Copyright © 2015 by the American Society of Neuroimaging.
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