| Literature DB >> 25691269 |
Dalveer Singh1, Charlie Chia-Tsong Hsu1, Gigi Nga Chi Kwan1, Ipeson Korah1.
Abstract
Pontine 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.Entities:
Keywords: Pontine cap tegmental dysplasia; vestibulocochlear nerve
Mesh:
Year: 2015 PMID: 25691269 DOI: 10.1111/jon.12209
Source DB: PubMed Journal: J Neuroimaging ISSN: 1051-2284 Impact factor: 2.486